Medical Device Manufacturer · US , San Diego , CA

Clonetics Corp.

4 submissions · 4 cleared · Since 1988
4
Total
4
Cleared
0
Denied

Clonetics Corp. — FDA 510(k) Submissions

Clonetics Corp. has submitted 4 FDA 510(k) premarket notifications since 1988, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Media And Components, Synthetic Cell And Tissue Culture . Use the specialty filter in the sidebar to narrow results.

4 devices
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All4 Pathology 4