Exigent Diagnostics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 9
Catalogue
Careside Analyzer Ref K982118
510(k) 510(k)Careside Glucose Ref K981183
510(k) 510(k)Careside Total Protein Ref K980042
510(k) 510(k)Careside Albumin Ref K980041
510(k) 510(k)Careside Creatinine Ref K980043
510(k) 510(k)Careside Bun Ref K980057
510(k) 510(k)Careside Hdl-Cholesterol Ref K981899
510(k) 510(k)Careside Analyzer Ref K980056
510(k) 510(k)Careside Globulin Ref K980055
510(k) 510(k)
Frequently asked questions
How many devices does Exigent Diagnostics, Inc. have in the registry?
The registry currently lists 9 devices for Exigent Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Exigent Diagnostics, Inc.'s devices?
Among its 9 most recently registered devices, Exigent Diagnostics, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Exigent Diagnostics, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Exigent Diagnostics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Exigent Diagnostics, Inc. in the registry?
The most recently registered devices listed for Exigent Diagnostics, Inc. include CARESIDE ANALYZER, CARESIDE GLUCOSE, CARESIDE TOTAL PROTEIN and CARESIDE ALBUMIN.