Wallach Surgical Devices, Inc. - FDA 510(k) Cleared Devices
27
Total
27
Cleared
0
Denied
Wallach Surgical Devices, Inc. has 27 FDA 510(k) cleared medical devices. Based in Walker, US.
Historical record: 27 cleared submissions from 1981 to 2002. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Wallach Surgical Devices, Inc. Filter by specialty or product code using the sidebar.
27 devices
Cleared
Jul 12, 2002
ENDOCERVICAL BLOCK NEEDLE
Obstetrics & Gynecology
86d
Cleared
Jun 03, 2002
WALLACH LOOP ELECTRODE
General & Plastic Surgery
90d
Cleared
Apr 11, 2000
WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR
Dental
33d
Cleared
Sep 29, 1999
WALLACH'S ULTIMATE REUSABLE, PLASTIC VAGINAL SPECULUM
Obstetrics & Gynecology
47d
Cleared
Aug 12, 1999
PMS 750 FINGERSWITCH
General & Plastic Surgery
90d
Cleared
May 20, 1999
WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR (PROPOSED)
Obstetrics & Gynecology
202d
Cleared
Mar 01, 1999
`THE INSEMINATOR' (PROPOSED)
Obstetrics & Gynecology
89d
Cleared
Feb 22, 1999
WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR
General & Plastic Surgery
161d
Cleared
Jun 11, 1997
WALLACH QUANTUM 2000 ELECTROSURGICAL SYSTEM
Obstetrics & Gynecology
272d
Cleared
Mar 19, 1997
WALLACH INTEGRATION UNIT
Obstetrics & Gynecology
205d
Cleared
Nov 22, 1995
WALLACH DIGITAL IMAGING SYSTEM
Radiology
282d
Cleared
May 04, 1995
WALLACH LEAP 100 ELECTRO SURGERY SYSTEM
Obstetrics & Gynecology
1115d