Crystal Diagnostics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Crystal Diagnostics, Inc. makes
Crystal Diagnostics, Inc. manufactures the CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST, which is a medical device used for measuring cholesterol levels in whole blood samples.
The company's products are regulated as Class I devices and are listed in the FDA 510(k) registry. Crystal Diagnostics, Inc. is based in the US.
Catalogue
Cholestat (Tm) Whole Blood Cholesterol Test Ref K910240
510(k) 510(k)Cholestat(Tm) Whole Blood Cholesterol Test Ref K903126
510(k) 510(k)
Frequently asked questions
How many devices does Crystal Diagnostics, Inc. have in the registry?
The registry currently lists 2 devices for Crystal Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Crystal Diagnostics, Inc.'s devices?
Among its 2 most recently registered devices, Crystal Diagnostics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Crystal Diagnostics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Crystal Diagnostics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Crystal Diagnostics, Inc. in the registry?
The most recently registered devices listed for Crystal Diagnostics, Inc. include CHOLESTAT (TM) WHOLE BLOOD CHOLESTEROL TEST and CHOLESTAT(TM) WHOLE BLOOD CHOLESTEROL TEST.