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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name cannula, surgical, general & plastic surgery
510(k) Number K903416
Device Name CANNULA, SURGICAL
Applicant
ADVANTAGE DIAGNOSTICS CORP
P.O. BOX 12428
TUCSON,  AZ  85732
Applicant Contact DANIEL P MISENHIMER
Correspondent
ADVANTAGE DIAGNOSTICS CORP
P.O. BOX 12428
TUCSON,  AZ  85732
Correspondent Contact DANIEL P MISENHIMER
Regulation Number878.4800
Classification Product Code
GEA  
Date Received07/30/1990
Decision Date 11/23/1990
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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