Gimmi GmbH is one of 68 FDA 510(k) medical device manufacturers from Netherlands in the dataset, ranked by real submission volume.
Gimmi GmbH - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Gimmi GmbH has 6 FDA 510(k) cleared medical devices. Based in Amsterdam, Nh, NL.
Historical record: 6 cleared submissions from 2001 to 2010.
Browse the FDA 510(k) cleared devices submitted by Gimmi GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Gimmi GmbH
6 devices
Cleared
Feb 12, 2010
ALPHAHYSTEROSCOPE, FIBEROPTIC, OPERATIVE AND DIAGNOSTIC
Obstetrics & Gynecology
189d
Cleared
Jan 27, 2010
ALPHAXENON LIGHT 180 W AND 300 W
Gastroenterology & Urology
117d
Cleared
May 06, 2009
GIMMI ANEURYSM CLIPS AND APPLYING FORCEPS
Neurology
329d
Cleared
Mar 11, 2002
GIMMI ALPHA HYSTEROSCOPES & ACCESSORIES, MODELS E.8XXX.XX, T.8XXX.XX,...
Obstetrics & Gynecology
196d
Cleared
Dec 20, 2001
GIMMI'ALPHA' ENDOSCOPES & ACCESSORIES
Gastroenterology & Urology
129d
Cleared
Nov 27, 2001
GIMMI ALPHA SINUSCOPES MODEL # E.8282.01/31/71 + E.8284.01/31/71
Ear, Nose, Throat
18d