Medical Device Manufacturer · US , Seattle , WA

Ostex Intl., Inc.

5 submissions · 5 cleared · Since 1995
5
Total
5
Cleared
0
Denied

Ostex Intl., Inc. — FDA 510(k) Submissions

Ostex Intl., Inc. has submitted 5 FDA 510(k) premarket notifications since 1995, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Column Chromatography & Color Development, Hydroxyproline . Use the specialty filter in the sidebar to narrow results.

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