Medical Device Manufacturer · US , Walker , MI

Gesco Intl., Inc. - FDA 510(k) Cleared Devices

26 submissions · 22 cleared · Since 1978

Total

Cleared

Denied

Gesco Intl., Inc. has 22 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 22 cleared submissions from 1978 to 1995. Primary specialty: General Hospital.

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

Gesco Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Gesco Intl., Inc.

26 devices

1-12 of 26

Cleared Dec 15, 1995

PER-Q-CATH MID-LINE

K954422 · LJS

General Hospital · 85d

Cleared Aug 02, 1994

UMBILI-CATH

K940870 · FOS

General Hospital · 158d

Cleared Aug 02, 1994

UMBILI-CATH-S

K940953 · FOS

General Hospital · 154d

Cleared Jul 29, 1994

UMBILI-CATH-S-DL

K940952 · FOS

General Hospital · 150d

Cleared May 16, 1994

URI-CATH CATHETER

K941672 · GBM

Gastroenterology & Urology · 41d

Cleared May 11, 1994

THORA-CATH

K941232 · JOL

General Hospital · 57d

Cleared Apr 29, 1994

UMBILI-CATH-P

K940871 · FOS

General Hospital · 63d

PER-Q-CATH DRESSING CHANGE TRAY

K926063 · MCY

General & Plastic Surgery · 188d

Cleared Mar 16, 1993

PALA-NATE

K923591 · BTR

Anesthesiology · 239d

Cleared Jan 27, 1992

GESCO PER-Q-CATH CATHETER INTRODUCER

K915167 · DYB

Cardiovascular · 73d

Cleared Aug 14, 1991

OBSTETRICAL VACUUM CUP

K911326 · HDB

Obstetrics & Gynecology · 141d

Gesco Intl., Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Gesco Intl., Inc.

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