Medical Device Manufacturer · US , Chicago , IL

Gibeck Respiration - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1987

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Gibeck Respiration Anesthesiology ✕

6 devices

1-6 of 6

Cleared Jun 24, 1988

HUMID-VENT FILTER

Anesthesiology · 70d

Cleared Jun 16, 1988

HUMID-VENT 2 S FLEX

Anesthesiology · 62d

Cleared Jun 10, 1988

Anesthesiology · 56d

Cleared Nov 24, 1987

HUMID-VENT(R) 2 PORT

Anesthesiology · 69d

Cleared Nov 06, 1987

HUMID-VENT(R) MINI

Anesthesiology · 51d

Cleared Aug 03, 1987

Anesthesiology · 60d