Ultra Quest Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ultra Lyte Potassium Reagent Kit Ref K843454
Regimes: 510(k) Registry: 510(k)Ultra Lyte Sodium Reagent Kit Ref K843453
Regimes: 510(k) Registry: 510(k)Ultra Lyte Analyzer I 100 Ref K842315
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ultra Quest Diagnostics, Inc. have in the registry?
The registry currently lists 3 devices for Ultra Quest Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ultra Quest Diagnostics, Inc.'s devices?
Among its 3 most recently registered devices, Ultra Quest Diagnostics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ultra Quest Diagnostics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ultra Quest Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ultra Quest Diagnostics, Inc. in the registry?
The most recently registered devices listed for Ultra Quest Diagnostics, Inc. include ULTRA LYTE POTASSIUM REAGENT KIT, ULTRA LYTE SODIUM REAGENT KIT and ULTRA LYTE ANALYZER I 100.