Medical Device Manufacturer · US , Jacksonville , FL

Ja-Ru, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1993
6
Total
6
Cleared
0
Denied

Ja-Ru, Inc. has 6 FDA 510(k) cleared medical devices. Based in Jacksonville, US.

Historical record: 6 cleared submissions from 1993 to 1994. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Ja-Ru, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Ja-Ru, Inc.

6 devices
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