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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 K880669
Device Name L-5 PLASTIC SURGERY CANNULAS
Applicant
AMERICAN INSTRUMENT MANUFACTURER'S, INC.
P.O. BOX 690
EUREKA,  MO  63025
Applicant Contact TERRY L SANDERSON
Correspondent
AMERICAN INSTRUMENT MANUFACTURER'S, INC.
P.O. BOX 690
EUREKA,  MO  63025
Correspondent Contact TERRY L SANDERSON
Regulation Number878.4800
Classification Product Code
GEA  
Date Received02/18/1988
Decision Date 03/17/1988
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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