Medical Device Manufacturer · US , Hackensack , NJ

Biolectron, Inc.

1 submissions · 1 cleared · Since 1997
1
Total
1
Cleared
0
Denied

Biolectron, Inc. — FDA 510(k) Submissions

Biolectron, Inc. has submitted 1 FDA 510(k) premarket notifications since 1997, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Surgical, Orthopedic, Pneumatic Powered & Accessory/attachment . Use the specialty filter in the sidebar to narrow results.

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