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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name board, arm (with cover), sterile
510(k) Number K830018
Device Name SAFE-T ARM BOARD
Applicant
HARVEY A. TURNER, M.D.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Correspondent
HARVEY A. TURNER, M.D.
4221 Richmond Rd., N.W.
Walker,  MI  49534
Regulation Number878.3910
Classification Product Code
BTX  
Date Received01/03/1983
Decision Date 01/26/1983
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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