Medical Device Manufacturer · US , Olathe , KS

Osborn Laboratories, Inc.

2 submissions · 2 cleared · Since 1999
2
Total
2
Cleared
0
Denied

Osborn Laboratories, Inc. — FDA 510(k) Submissions

Osborn Laboratories, Inc. has submitted 2 FDA 510(k) premarket notifications since 1999, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Oral Fluid Drugs Of Abuse And Alcohol Test Specimen Collection Device, Assay, Glycosylated Hemoglobin . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Hematology 1 Chemistry 1