Medical Device Manufacturer · US , Walker , MI

Pneupac , Ltd. - FDA 510(k) Cleared Devices

19 submissions · 19 cleared · Since 1980

19

Total

19

Cleared

0

Denied

FDA 510(k) Regulatory Record - Pneupac , Ltd. Cardiovascular ✕

4 devices

1-4 of 4

Cleared Feb 05, 1980

PNEUPAC RESUSCITATOR INSTANT ACTION SET

Cardiovascular · 64d

Cleared Feb 05, 1980

PNEUPAC RESUSCITATOR INSTANT ACTION SET

Cardiovascular · 64d

Cleared Feb 05, 1980

PNEUPAC RESUSCITATOR INSTANT ACTION SET

Cardiovascular · 64d

Cleared Feb 05, 1980

PNEUPAC TEST SET, PT.#500-A250

Cardiovascular · 64d