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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Test, Time, Prothrombin
510(k) Number K780203
Device Name THROMBOPLASTIN DRIED
Applicant
Hyland Therapeutic Div., Travenol Laboratories
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Hyland Therapeutic Div., Travenol Laboratories
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number864.7750
Classification Product Code
GJS  
Date Received02/07/1978
Decision Date 03/27/1978
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Hematology
510k Review Panel Hematology
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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