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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name light, ultraviolet, dermatological
510(k) Number K845029
Device Name SURGICAL POWER MAGNET
Applicant
FRIEDMAN LABS, INC.
P.O. BOX 5360
BALTIMORE,  MD  21209
Applicant Contact AARON FRIEDMAN
Correspondent
FRIEDMAN LABS, INC.
P.O. BOX 5360
BALTIMORE,  MD  21209
Correspondent Contact AARON FRIEDMAN
Regulation Number878.4630
Classification Product Code
FTC  
Date Received12/27/1984
Decision Date 05/10/1985
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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