Medical Device Manufacturer · US , Princeton , NJ

Princeton Regulatory Assoc.

4 submissions · 4 cleared · Since 1996
4
Total
4
Cleared
0
Denied

Princeton Regulatory Assoc. — FDA 510(k) Submissions

Princeton Regulatory Assoc. has submitted 4 FDA 510(k) premarket notifications since 1996, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Alarm, Conditioned Response Enuresis, Warmer, Irrigation Solution, Pump, Infusion, Elastomeric, Stent, Ureteral . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
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