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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 K871043
Device Name (I) LV AND (II) HV SERIES CANNULA
Applicant
CELEBRATION MEDICAL PRODUCTS, INC.
900 WELCH RD.
SUITE 20
PALO ALTO,  CA  94304
Applicant Contact WEBER, JR.,MD
Correspondent
CELEBRATION MEDICAL PRODUCTS, INC.
900 WELCH RD.
SUITE 20
PALO ALTO,  CA  94304
Correspondent Contact WEBER, JR.,MD
Regulation Number878.4800
Classification Product Code
GEA  
Date Received03/17/1987
Decision Date 04/23/1987
Decision SUBSTANTIALLY EQUIVALENT FOR SOME INDICATIONS (SN)
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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