Medical Device Manufacturer · US , Indianapolis , IN

Gibeck, Inc. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 1990

15

Total

15

Cleared

0

Denied

FDA 510(k) Regulatory Record - Gibeck, Inc. Anesthesiology ✕

9 devices

1-9 of 9

Cleared Aug 25, 1995

HUMID-VENT 1 PORT/HUMID-VENT 1 PORT ANGLE

Anesthesiology · 31d

Cleared Aug 25, 1995

HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHT

Anesthesiology · 28d

Cleared Jul 25, 1995

HUMID-VENT TRACH-VENT

Anesthesiology · 34d

Cleared Jul 20, 1995

Anesthesiology · 35d

Cleared Jul 20, 1995

Anesthesiology · 29d

Cleared Jun 12, 1995

HUMID-VENT FILTER PEDI

Anesthesiology · 40d

Cleared Jun 07, 1995

HUMID-VENT MICRO

Anesthesiology · 47d

Cleared Mar 16, 1990

GAS SAMPLING NASAL CANNULA

Anesthesiology · 14d

Cleared Mar 13, 1990

DISPOSABLE CO2 ABSORBER/E

Anesthesiology · 75d