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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name forceps, general & plastic surgery
510(k) Number K891401
Device Name HEMOSTATIC FORCEPS BRUNS.,GEMINI,SPENCER-WELL,KANT
Applicant
ZINNANTI SURGICAL INSTRUMENTS, INC.
21540-B PRAIRIE ST.
CHATSWORTH,  CA  91311
Applicant Contact ANNA STRAIGHT
Correspondent
ZINNANTI SURGICAL INSTRUMENTS, INC.
21540-B PRAIRIE ST.
CHATSWORTH,  CA  91311
Correspondent Contact ANNA STRAIGHT
Regulation Number878.4800
Classification Product Code
GEN  
Date Received03/14/1989
Decision Date 04/06/1989
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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