Control Medical Technology
United Statesfrom the FDA registration address FDA establishment FEI 3031788372
- Devices
- 4
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Aspire Mechanical Aspirator G Ref K200629
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Aspire Rx-LP6 Aspiration Catheter Ref K131998
Regimes: 510(k) Registry: 510(k)Aspire Max Aspiration Catheter Ref K113757
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3031788372
- Address
- 2490 S 300 W, South Salt Lake, UT, 84115
Frequently asked questions
How many devices does CONTROL MEDICAL TECHNOLOGY have in the registry?
The registry currently lists 4 devices for CONTROL MEDICAL TECHNOLOGY. Devices recorded under merged duplicate company entries are counted once.
Which registries list CONTROL MEDICAL TECHNOLOGY's devices?
Among its 4 most recently registered devices, CONTROL MEDICAL TECHNOLOGY has devices listed in FDA 510(k) (4 devices).
What risk classes do CONTROL MEDICAL TECHNOLOGY's devices fall under?
Among its 4 most recently registered devices, the classes recorded for CONTROL MEDICAL TECHNOLOGY's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CONTROL MEDICAL TECHNOLOGY in the registry?
The most recently registered devices listed for CONTROL MEDICAL TECHNOLOGY include Aspire Mechanical Aspirator G, Aspire MAX 7 - 11F Mechanical Thrombectomy System and Aspire Mechanical Aspirator, ASPIRE RX-LP6 ASPIRATION CATHETER and ASPIRE MAX ASPIRATION CATHETER.