Data / Medical devices / United States / Fukuda Denshi Usa, Inc.
Fukuda Denshi Usa, Inc.: FDA-registered device maker in Redmond, WA, United States, 26 510(k) clearances
Fukuda Denshi Usa, Inc. is registered with the FDA (registration 3031158) in Redmond, WA, United States. It lists 18 device types. The FDA files 26 510(k) clearances under its listings, the newest dated April 16, 2018. 1 recall event names it as the recalling firm. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3031158
- FEI number
- 3000215024
- Address
- 17725 N.E. 65TH ST., BLDG. C, Redmond, WA, United States, 98052
- Owner or operator
- Fukuda Denshi Co., Ltd. (9028352)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- January 16, 2008
- Registered through
- 2026
- Brand names listed
- CardiMax FX-8000/9000 Series ECG, DYNASCOPE 2000 Series BDS-2100 System, DynaScope DS-5000 Series Central Station, DynaScope DS-8000 Series Patient Monitors, DynaScope DS-8100 Series, FD DMS Software, FD DS-5000 CS, FD DS-5000 Series Telemetry and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 16, 2018 | K173226 | CardiMax Electrocardiograph | DPS | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| March 16, 2015 | K150030 | Fukuda Denshi DynaScope Model DS-8000 Series Patient Monitor | MHX | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| February 12, 2015 | K134046 | FUKUDA DENSHI DYNASCOPE MODEL DS-8100N/8100M PATIENT MONITOR | MHX | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| December 21, 2011 | K112521 | FUKUDA DENSHI VASERA MODEL VS-1500 | DXN | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| April 8, 2011 | K110920 | UF-760AG | ITX | Substantially Equivalent | Fukuda Denshi Co., Ltd. | accessdata.fda.gov |
| March 11, 2011 | K103134 | FUKUDA DENSHI | MHX | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| March 19, 2009 | K083697 | FUKUDA DENSHI DYNASCOPE MODEL DS-7000 SERIES PATIENT MONITOR, MODEL DS-7000//7000M/7210/7210M | MHX | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| September 30, 2008 | K082656 | MODEL FF SONIC US-750 XT DIAGNOSTIC ULTRASOUND SYSTEM 3D IMAGING UNIT | IYN | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| September 9, 2008 | K081919 | UF-870 AG DIAGNOSTIC ULTRASOUND SYSTEM | ITX | Substantially Equivalent | Fukuda Denshi Co., Ltd. | accessdata.fda.gov |
| August 29, 2008 | K081891 | FUKUDA DENSHI DYNASCOPE MODEL DS-7000/7000M PATIENT MONITOR | MHX | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| June 14, 2006 | K061437 | SIGMA 5000 SERIES, IMAGIC | IYN | Substantially Equivalent | Kontron Medical Systems Sas | accessdata.fda.gov |
| February 17, 2005 | K050363 | FUKUDA DENSHI MODEL UF-850XTD | IYN | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| June 3, 2004 | K033711 | FUKUDA DENSHI DYNASCOPE MODEL DS-5000 CENTRAL TELEMETRY SYSTEM | MHX | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| May 26, 2004 | K040246 | FUKUDA DENSHI DYNASCOPE MODEL DS-7141 PORTABLE PATIENT MONITOR | MHX | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| October 31, 2003 | K033209 | FUKUDA DENSHI MODEL FF SONIC UF-750XT | IYN | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| October 10, 2003 | K032290 | FUKUDA DENSHI DYNASCOPE MODEL DS-7100 SERIES PORTABLE PATIENT MONITOR | MHX | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| February 6, 2002 | K020084 | FUKUDA DENSHI DYNASCOPE MODEL DS-5700 | DSI | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| December 20, 2001 | K013273 | FUKUDA DENSHI MODEL HG-500, PULSE OXIMETER MODULE | DQA | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| April 7, 2000 | K000746 | FUKUDA DENSHI DYNASCOPE, MODEL DS-5800NX | DSI | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| October 15, 1999 | K990401 | FUKUDA DENSHI FF SONIC UF-5800 GENERAL PURPOSE ULTRASOUND SCANNING SYSTEM WITH DOPPLER | IYO | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| August 31, 1998 | K981066 | FUKUDA DENSHI: CARDIOMAX, MODEL FX-4010 MULTI CHANNEL ELECTROCARDIOGRAPH | LOS | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| June 19, 1998 | K980728 | FUKUDA DENSHI DYNASCOPE MODEL DS-5000 SERIES TELEMETRY SYSTEM | DSI | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| December 2, 1997 | K971440 | FUKUDA DENSHI MODEL FCP-2155 MULTI CHANNEL, INTERPRETIVE ELECTROCARDIOGRAPH | LOS | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| September 9, 1997 | K970585 | FUKUDA DENSHI DYNASCOPE MODEL DS-5800 CENTRAL STATION MONITOR | DSI | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| May 1, 1997 | K964187 | FUKADA DENSHI DYNASCOPE MODEL DS-5300 PATIENT MONITOR | DSI | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
| August 30, 1993 | K922208 | FUKUDA DENSHI MODEL UF-4500 | IYO | Substantially Equivalent | Fukuda Denshi USA, Inc. | accessdata.fda.gov |
Recalls
Recall events where this establishment is the recalling firm, matched on its FEI.
| Initiated | Event | Class | Status | Product | Reason | Source |
|---|---|---|---|---|---|---|
| December 21, 2015 | 72953 | Class II | Terminated | Fukuda Denshi patient monitor model DS-8100M and DS-8100N. The Fukuda Denshi DynaScope Model DS-8100N/8100M Patient Monitor is meant to acquire and monitor physiological signals from patients. | A possible malfunction where a Short-term Battery Error message has appeared and has been traced back to a bad (damaged) Lithium-Ion capacitor (Short-term Backup battery). | accessdata.fda.gov |
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Updated April 16, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.