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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Apparatus, Autotransfusion
510(k) Number K890171
Device Name INLINE AUTOTRANSFUSION SYSTEM
Applicant
Conmedcorp
310 Broad St.
Utica,  NY  13501
Applicant Contact WILLIAM W ABRAHAM
Correspondent
Conmedcorp
310 Broad St.
Utica,  NY  13501
Correspondent Contact WILLIAM W ABRAHAM
Regulation Number868.5830
Classification Product Code
CAC  
Date Received01/17/1989
Decision Date 06/15/1989
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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