Medical Device Manufacturer · US , Camp Hill , PA

Gi Supply - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1992

Recent clearances: EverLift Submucosal Lifting Agent

8

Total

8

Cleared

0

Denied

Gi Supply has 8 FDA 510(k) cleared medical devices. Based in Camp Hill, US.

Historical record: 8 cleared submissions from 1992 to 2020.

Browse the FDA 510(k) cleared devices submitted by Gi Supply Filter by specialty or product code using the sidebar.

Gi Supply 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 - Gi Supply

8 devices

1-8 of 8

Cleared Jun 20, 2020

EverLift Submucosal Lifting Agent

Gastroenterology & Urology · 338d

Cleared Sep 24, 2003

GI SUPPLY BILIARY STENT

Gastroenterology & Urology · 147d

Cleared Sep 25, 2001

Microbiology · 57d

Cleared Feb 14, 1997

GI SUPPLY PARACENTESIS PUMP

General & Plastic Surgery · 28d

Cleared Feb 14, 1997

RUNYON LARGE VOLUME PARACENTESIS KIT

General & Plastic Surgery · 28d

Cleared Apr 20, 1995

Microbiology · 198d

Cleared Oct 04, 1993

Gastroenterology & Urology · 217d

Cleared Mar 27, 1992

BITE BLOCK/MOUTHPIECE FOR ENDOSCOPY

Ear, Nose, Throat · 88d