Medical Device Manufacturer · US , Sandpoint , ID

Percussionaire Corp. - FDA 510(k) Cleared Devices

11 submissions · 9 cleared · Since 1989

11

Total

9

Cleared

0

Denied

FDA 510(k) Regulatory Record - Percussionaire Corp. Dental ✕

1 devices

1-1 of 1

Cleared Jan 09, 1990

RATE INCREASE FOR IPPB/IPV