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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
510(k) Number K841880
Device Name ERYTHROCATH UMBILICAL CATHETER
Applicant
Cardio Search, Inc.
P.O. Box 24126
Tampa,  FL  33623
Applicant Contact LARRY H BRIM
Correspondent
Cardio Search, Inc.
P.O. Box 24126
Tampa,  FL  33623
Correspondent Contact LARRY H BRIM
Regulation Number880.5200
Classification Product Code
FOZ  
Date Received05/07/1984
Decision Date 01/14/1985
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty General Hospital
510k Review Panel General Hospital
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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