Data / Medical devices / Norway / Medistim Asa
Medistim Asa: FDA-registered device maker in HORTEN Vestfold, Norway, 3 510(k) clearances
Medistim Asa is registered with the FDA (registration 3003647374) in HORTEN Vestfold, Norway. It lists 6 device types. The FDA files 3 510(k) clearances under its listings, the newest dated December 27, 2010. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003647374
- Address
- Bromsveien 17, HORTEN Vestfold, Norway, 3183
- Owner or operator
- Medistim ASA (9038441)
- Roles
- Manufacturer
- First device listed
- December 10, 2007
- Registered through
- 2026
- Brand names listed
- Medi-Stim Butterfly Flowmeter, Medistim Doppler Probe, Medistim Imaging probe, Medistim MiraQ system, Medistim Transit-Time Probe, Medistim VeriQ System, Medistim VeriQC system
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Computer, Blood-Pressure | DSK | 2 | Manufacturer | accessdata.fda.gov |
| Flowmeter, Blood, Cardiovascular | DPW | 2 | Manufacturer | accessdata.fda.gov |
| Probe, Blood-Flow, Extravascular | DPT | 2 | Manufacturer | accessdata.fda.gov |
| System, Imaging, Pulsed Doppler, Ultrasonic | IYN | 2 | Manufacturer | accessdata.fda.gov |
| System, Imaging, Pulsed Echo, Ultrasonic | IYO | 2 | Manufacturer | accessdata.fda.gov |
| Transducer, Ultrasonic, Diagnostic | ITX | 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 |
|---|---|---|---|---|---|---|
| December 27, 2010 | K102595 | MEDISTIM VERIQC SYSTEM | DPW | Substantially Equivalent | Medi-Stim Asa | accessdata.fda.gov |
| April 29, 2004 | K040228 | MEDI-STIM VERIQ SYSTEM, MODEL VQ1001 - VQ4122 | DPW | Substantially Equivalent | Medi-Stim A/S | accessdata.fda.gov |
| September 8, 1999 | K992305 | MEDI-STIM BUTTERFLY FLOWMETER, MODEL BF1000-BF2004 | ITX | Substantially Equivalent | Medi-Stim A/S | accessdata.fda.gov |
Compare with other makers
- All makers of Flowmeter, Blood, Cardiovascular
- All makers of Transducer, Ultrasonic, Diagnostic
- All makers of System, Imaging, Pulsed Echo, Ultrasonic
- All makers of System, Imaging, Pulsed Doppler, Ultrasonic
- All makers of Probe, Blood-Flow, Extravascular
- All makers of Computer, Blood-Pressure
Updated December 27, 2010. 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.