Osborn Group, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Osborn Group, Inc. makes
Osborn Group, Inc. makes sample collection kits for diagnostic testing, including the APPRAISE-CARDIO SAMPLE COLLECTION KIT, HEMOCHEK-A1C SAMPLE COLLECTION KIT, HEMOCHEK URINE COLLECTION KIT, and APPRAISE URINE MICROALBUMIN COLLECTION KIT.
These devices 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
Appraise-Cardio Sample Collection Kit Ref K993787
Regimes: 510(k) Registry: 510(k)Hemochek-A1C Sample Collection Kit Ref K990899
Regimes: 510(k) Registry: 510(k)Hemochek Urine Collection Kit Ref K991800
Regimes: 510(k) Registry: 510(k)Appraise Urine Microalbumin Collection Kit Ref K002156
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Osborn Group, Inc. have in the registry?
The registry currently lists 4 devices for Osborn Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Osborn Group, Inc.'s devices?
Among its 4 most recently registered devices, Osborn Group, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Osborn Group, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Osborn Group, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Osborn Group, Inc. in the registry?
The most recently registered devices listed for Osborn Group, Inc. include APPRAISE-CARDIO SAMPLE COLLECTION KIT, HEMOCHEK-A1C SAMPLE COLLECTION KIT, HEMOCHEK URINE COLLECTION KIT and APPRAISE URINE MICROALBUMIN COLLECTION KIT.