Alltek, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Manual Irrigating/Aspirating Unit Ref K840495
Regimes: 510(k) Registry: 510(k)I.V. Watch Ref K854172
Regimes: 510(k) Registry: 510(k)Filtrare Tm Allvent Tm Ref K834376
Regimes: 510(k) Registry: 510(k)Pediatric Iv Watch Ref K852030
Regimes: 510(k) Registry: 510(k)I.V. Watch Ref K852029
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alltek, Inc. have in the registry?
The registry currently lists 5 devices for Alltek, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alltek, Inc.'s devices?
Among its 5 most recently registered devices, Alltek, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Alltek, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Alltek, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Alltek, Inc. in the registry?
The most recently registered devices listed for Alltek, Inc. include MANUAL IRRIGATING/ASPIRATING UNIT, I.V. WATCH, FILTRARE TM ALLVENT TM and PEDIATRIC IV WATCH.