Medical Device Manufacturer · US , Indianapolis , IN

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

15 submissions · 15 cleared · Since 1990

Total

Cleared

Denied

Gibeck, Inc. has 15 FDA 510(k) cleared medical devices. Based in Indianapolis, US.

Historical record: 15 cleared submissions from 1990 to 1997. Primary specialty: Anesthesiology.

Browse the FDA 510(k) cleared devices submitted by Gibeck, Inc. Filter by specialty or product code using the sidebar.

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

15 devices

1-12 of 15

Cleared Dec 02, 1997

ISO-GARD FILTER ANGLED(18212)/ISO-GARD FILTER STRAIGHT(19212)

K965016 · CAH

General Hospital · 351d

Cleared Apr 23, 1997

THERMAL REGULATION SYSTEM BLANKET

K964377 · DWJ

Cardiovascular · 173d

Cleared Apr 15, 1997

HUMID-VENT FILTER COMPACT ANGLED (18402)/HUMID-VENT FILTER COMPACT...

K964382 · CAH

General Hospital · 162d

Cleared Jan 13, 1997

GIBECK WARMBAG REUSABLE CONVECTIVE WARMING BLANKET

K960511 · DWJ

Cardiovascular · 343d

Cleared May 02, 1996

ISO-GARD HEPA FILTER-HME, ISO-ARD HEPA FILTER-HME W/PORT

K954828 · CAH

General Hospital · 195d

Cleared Aug 25, 1995

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

K953491 · BYD

Anesthesiology · 31d

Cleared Aug 25, 1995

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

K953544 · BYD

Anesthesiology · 28d

Cleared Jul 25, 1995

HUMID-VENT TRACH-VENT

HUMID-VENT FILTER PEDI

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

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