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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
Predetermined Change
Control Plan Authorized		 No
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