Endocrine Associates, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Endocrine Associates, Inc. makes
Endocrine Associates, Inc. manufactures radioimmunoassay (RIA) kits for measuring calcitonin and dehydroepiandrosterone sulfate (DHEA‑S) in clinical samples.
These kits are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Calcitonin Ria Kit Ref K872880
Regimes: 510(k) Registry: 510(k)Dhea-S Ria Kit Ref K872879
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endocrine Associates, Inc. have in the registry?
The registry currently lists 2 devices for Endocrine Associates, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endocrine Associates, Inc.'s devices?
Among its 2 most recently registered devices, Endocrine Associates, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Endocrine Associates, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Endocrine Associates, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endocrine Associates, Inc. in the registry?
The most recently registered devices listed for Endocrine Associates, Inc. include CALCITONIN RIA KIT and DHEA-S RIA KIT.