Gastrotech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Gastrotech, Inc. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Gastrotech, Inc. has 4 FDA 510(k) cleared medical devices. Based in Independence, US.
Historical record: 4 cleared submissions from 1986 to 1989. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Gastrotech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gastrotech, Inc.
5 devices
Cleared
Oct 03, 1989
SYRINGE INJECTION GUN DELIVERY KITS
General & Plastic Surgery
237d
Cleared
May 31, 1989
ESOPHAGEAL OVERTUBE
Gastroenterology & Urology
110d
Cleared
Aug 23, 1988
GASTROSTOMY FEEDING TUBE
Gastroenterology & Urology
14d
Cleared
Aug 23, 1988
PERCUTANEOUS ENDOSCOPIC GASTROSTOMY FEEDING TUBE
Gastroenterology & Urology
14d
Cleared
Aug 06, 1986
SYRINGE INJECTION GUN
General & Plastic Surgery
8d