Wilson Greatbatch Technologies, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Wilson Greatbatch Technologies, Inc. has 9 FDA 510(k) cleared medical devices. Based in Clarence, US.
Historical record: 9 cleared submissions from 1994 to 1998. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Wilson Greatbatch Technologies, Inc. Filter by specialty or product code using the sidebar.
9 devices
Cleared
May 13, 1998
GREATBATCH SCIENTIFIC MR COMPATIBLE HYSTEROSCOPE
Obstetrics & Gynecology
394d
Cleared
Apr 30, 1998
GREATBATCH SCIENTIFIC MR COMPATIBLE LARYNGOSCOPE
Anesthesiology
381d
Cleared
Dec 11, 1997
GREATBATCH SCIENTIFIC MR COMPATIBLE LAPAROSCOPES AND OPERATING LAPAROSCOPES
General & Plastic Surgery
176d
Cleared
Nov 21, 1997
GREATBATCH SCIENTIFIC MR COMPATIBLE ARTHROSCOPES AND SMALL JOINT ARTHROSCOPES
Orthopedic
191d
Cleared
Nov 19, 1997
GREATBATCH SCIENTIFIC MRI COMPATIBLE FIBER OPTIC LARYNGOSCOPE HANDLE
Anesthesiology
274d
Cleared
Oct 31, 1997
GREATBATCH SCIENTIFIC MR COMPATIBLE SINUSCOPE
Ear, Nose, Throat
200d
Cleared
Dec 22, 1995
WGL ENDOSCOPIC GRASPER W/DETACHABLE STRAP
General & Plastic Surgery
73d
Cleared
Jan 27, 1995
WGL ENDOSCOPIC GRASPER*
General & Plastic Surgery
21d
Cleared
Dec 13, 1994
WGL ENDOSCOPIC GRASPER
General & Plastic Surgery
223d