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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Kit, Quality Control For Blood Banking Reagents
510(k) Number K780665
Device Name RECAP
Applicant
Bca Biological Corp. of America
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Bca Biological Corp. of America
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number864.9650
Classification Product Code
KSF  
Date Received04/21/1978
Decision Date 06/06/1978
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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