Medical Device Manufacturer · US , Mchenry , IL

Corpak Co. - FDA 510(k) Cleared Devices

21 submissions · 20 cleared · Since 1981

21

Total

20

Cleared

0

Denied

FDA 510(k) Regulatory Record - Corpak Co. Anesthesiology ✕

5 devices

1-5 of 5

Cleared Apr 29, 1982

Anesthesiology · 23d

Cleared Mar 17, 1981

Anesthesiology · 14d

Cleared Mar 04, 1981

NEBULIZER HEATER

Anesthesiology · 36d

Cleared Mar 04, 1981

PREFILLED NEBULIZER

Anesthesiology · 36d

Cleared Mar 04, 1981

PREFILLED HUMIDIFER

Anesthesiology · 36d