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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 K922460
Device Name ORIGIN SECONDARY CANNULA AND TROCAR
Applicant
Origin Medsystems, Inc.
1021 Howard Ave.
San Carlos,  CA  94070
Applicant Contact ALBERT K CHIN
Correspondent
Origin Medsystems, Inc.
1021 Howard Ave.
San Carlos,  CA  94070
Correspondent Contact ALBERT K CHIN
Regulation Number878.4800
Classification Product Code
GEA  
Date Received05/26/1992
Decision Date 09/16/1992
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
Predetermined Change
Control Plan Authorized		 No
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