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Wallach Surgical Devices, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
27
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K021224ENDOCERVICAL BLOCK NEEDLEJuly 12, 2002
K020711WALLACH LOOP ELECTRODEJune 3, 2002
K000768WALLACH QUANTUM 500 ELECTROSURGICAL GENERATORApril 11, 2000
K992736WALLACH'S ULTIMATE REUSABLE, PLASTIC VAGINAL SPECULUMSeptember 29, 1999
K991669PMS 750 FINGERSWITCHAugust 12, 1999
K983840WALLACH QUANTUM 500 ELECTROSURGICAL GENERATOR (PROPOSED)May 20, 1999
K984306`THE INSEMINATOR' (PROPOSED)March 1, 1999
K983208WALLACH QUANTUM 500 ELECTROSURGICAL GENERATORFebruary 22, 1999
K963653WALLACH QUANTUM 2000 ELECTROSURGICAL SYSTEMJune 11, 1997
K963348WALLACH INTEGRATION UNITMarch 19, 1997
K950630WALLACH DIGITAL IMAGING SYSTEMNovember 22, 1995
K921791WALLACH LEAP 100 ELECTRO SURGERY SYSTEMMay 4, 1995
K943201CLEAN AIRFebruary 28, 1995
K935634WALLACH LEEP PROCEDURE KITJuly 20, 1994
K935010WALLACH ULTRA FREEZEFebruary 9, 1994
K910491WALLACH COLD SOAKERMay 21, 1991
K902693WALLACH FLEXIBLE ENDOMETRIAL SAMPLERJanuary 31, 1991
K896065WALLACH CC/BRUSHJanuary 4, 1990
K880416WCCS 800 WALLACH CARDIAC CRYOSURGICAL SYSTEMSeptember 26, 1988
K871683COLPOSTAR V-6August 5, 1987