Gainor Medical Europe, Ltd. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Gainor Medical Europe, Ltd. has 13 FDA 510(k) cleared medical devices. Based in Mcdonough, US.
Historical record: 13 cleared submissions from 1990 to 1994.
Browse the FDA 510(k) cleared devices submitted by Gainor Medical Europe, Ltd. Filter by specialty or product code using the sidebar.
13 devices
Cleared
May 02, 1994
I.V. ADMINISTRATION SET
General Hospital
495d
Cleared
Oct 15, 1993
CARELET SAFETY LANCET
General & Plastic Surgery
190d
Cleared
Sep 13, 1993
CLEANLET, CLEANLET XL & KIDS
General & Plastic Surgery
158d
Cleared
Aug 10, 1993
SURESEAL BANDAGE
General & Plastic Surgery
445d
Cleared
Oct 23, 1991
I.V. PRIMING SET
General Hospital
89d
Cleared
Jun 06, 1991
NEEDLE, ASPIRATION & INJECTION, DISPOSABLE
General Hospital
371d
Cleared
Apr 17, 1991
CATHETER, NASAL, OXYGEN
Anesthesiology
321d
Cleared
Mar 01, 1991
NEEDLE, DIALYSIS
Gastroenterology & Urology
263d
Cleared
Nov 20, 1990
STOMACH, GASTRO-ENTEROSTOMY
Gastroenterology & Urology
173d
Cleared
Nov 20, 1990
HEMODIALYSIS SYSTEM AND ACCESSORY
Gastroenterology & Urology
173d
Cleared
Aug 01, 1990
SURELITE AND SURELITE XL BLOOD LANCET
General & Plastic Surgery
62d
Cleared
Jul 16, 1990
BAG, URINE
Gastroenterology & Urology
46d