Pneupac , Ltd.
Pneupac , Ltd. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 2004.
Top product codes for Pneupac , Ltd.
Recent clearances by Pneupac , Ltd.
- K040090 — COMPPAC 200HD; CS12 POWER SUPPLY (AIRCRAFT/VECHILE); PS11 POWER SUPPLY (MAINS)
- K030803 — PARAPAC 200D TRANSPORT, MODEL V200D
- K021841 — COMPPAC VENTILATOR MODELS 200 & PS11 POWER SUPPLY/CHARGER
- K020899 — PARAPAC 200 MEDIC, MODEL P200, & PARAPAC 200D MEDIC, MODEL P200D
- K960515 — PARAPAC
- K863410 — PATIENT VALVE WITH AIR ENTRAINMENT
- K862830 — MODELS 2R AND 3R PNEUPAC VENTILATOR/RESUSCITATOR
- K843737 — PNEUPAC INSTANT ACTION VENTILATOR/RESUS
- K832700 — PNEU PAC VENTILATOR/RESUSCITATORS
- K820220 — VENTILATOR MODELS
- K792451 — PNEUPAC RESUSCITATOR INSTANT ACTION SET
- K792452 — PNEUPAC RESUSCITATOR INSTANT ACTION SET
- K792453 — PNEUPAC OXYGEN THERAPY UNIT
- K792454 — PNEUPAC RESUSCITATOR INSTANT ACTION SET
- K792455 — PNEUPAC VENTILATOR/RESUSCITATOR #2
- K792456 — PNEUPAC VENTILATOR/RESUSCITATOR #3
- K792457 — COMPRESSOR
- K792458 — PNEUPAC TEST SET, PT.#500-A250
- K792459 — PNEUPAC VENTILATOR/RESUSCITATOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.