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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Razor, Surgical
510(k) Number K946162
Device Name 3M(TM) SURGICAL SLIPPER, 9660 SERIES
Applicant
Wahl Clipper Corp.
2900 N. Locust St.
P.O. Box 578
Steriling,  IL  61081 -0578
Applicant Contact CYNTHIA DE LONG
Correspondent
Wahl Clipper Corp.
2900 N. Locust St.
P.O. Box 578
Steriling,  IL  61081 -0578
Correspondent Contact CYNTHIA DE LONG
Regulation Number878.4800
Classification Product Code
LWK  
Date Received12/19/1994
Decision Date 01/24/1995
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General & Plastic Surgery
510k Review Panel General & Plastic Surgery
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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