Data / Medical devices / United States / Nasiff Assoc., Inc.
Nasiff Assoc., Inc.: FDA-registered device maker in Central Square, NY, United States, 4 510(k) clearances
Nasiff Assoc., Inc. is registered with the FDA (registration 1319390) in Central Square, NY, United States. It lists 4 device types. The FDA files 4 510(k) clearances under its listings, the newest dated April 10, 2000. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1319390
- Address
- 841-1 County Route 37, Central Square, NY, United States, 13036
- Owner or operator
- NASIFF ASSOC., INC. (9001556)
- Roles
- Contract manufacturer, Manufacturer
- First device listed
- March 1, 2007
- Registered through
- 2026
- Brand names listed
- CARDIO-CARD, Cardio Card Holter, Cardio NIBP, Cardio Suite
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Electrocardiograph | DPS | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| LOS | LOS | Manufacturer | accessdata.fda.gov | |
| Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm) | DRT | 2 | Manufacturer | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Manufacturer | accessdata.fda.gov |
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 10, 2000 | K993616 | CARDIO-CARD INTERPRETATION SYSTEM I | LOS | Substantially Equivalent | Nasiff Assoc., Inc. | accessdata.fda.gov |
| February 20, 1998 | K972795 | CARDIO-CARD MANAGEMENT SYSTEM II | DXN | Substantially Equivalent | Nasiff Assoc., Inc. | accessdata.fda.gov |
| August 7, 1996 | K960544 | CARDIO-CARD HOLTER ECG MANAGEMENT SYSTEM | DRT | Substantially Equivalent | Nasiff Assoc., Inc. | accessdata.fda.gov |
| July 9, 1992 | K920020 | CARDIO-CARD ECG MANAGEMENT SYSTEM | DPS | Substantially Equivalent | Nasiff Assoc., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of LOS
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Monitor, Cardiac (Incl. Cardiotachometer & Rate Alarm)
- All makers of Electrocardiograph
Updated April 10, 2000. 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.