Wallach Surgical Devices, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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.
FDA 510(k) Regulatory Record - Wallach Surgical Devices, Inc.
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