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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Table, Operating-Room, Ac-Powered
510(k) Number K932186
Device Name BYPASS LEG POSITIONER
Applicant
VOSS MEDICAL PRODUCTS
1920 N STREET,N.W.
SUITE 650
WASHINGTON,  DC  20036
Applicant Contact BRUCE MACKLER
Correspondent
VOSS MEDICAL PRODUCTS
1920 N STREET,N.W.
SUITE 650
WASHINGTON,  DC  20036
Correspondent Contact BRUCE MACKLER
Regulation Number878.4960
Classification Product Code
FQO  
Date Received05/05/1993
Decision Date 06/01/1993
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
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