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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name System, Automated Platelet Aggregation
510(k) Number K770395
Device Name THROMBO-CETIN (RISTOCETIN)
Applicant
Bay Area Hema. Onco. Clinic. & Res. L
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Bay Area Hema. Onco. Clinic. & Res. L
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number864.5700
Classification Product Code
JOZ  
Date Received02/28/1977
Decision Date 03/21/1977
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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