Medical Device Manufacturer · US , Fort Worth , TX

Bova Intl.

2 submissions · 2 cleared · Since 1994
2
Total
2
Cleared
0
Denied

Bova Intl. — FDA 510(k) Submissions

Bova Intl. has submitted 2 FDA 510(k) premarket notifications since 1994, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Anomaloscope, Lens, Guide, Intraocular . Use the specialty filter in the sidebar to narrow results.

2 devices
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