Medical Device Manufacturer · US , Chicago , IL

Zetek, Inc.

1 submissions · 1 cleared · Since 1985
1
Total
1
Cleared
0
Denied

Zetek, Inc. — FDA 510(k) Submissions

Zetek, Inc. has submitted 1 FDA 510(k) premarket notifications since 1985, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Test, Luteinizing Hormone (lh), Over The Counter . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
Filters
Filter by Specialty
All1 Toxicology 1