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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Radioassay, Vitamin B12
510(k) Number K760946
Device Name B12/FOLATE SING. TUBE DUAL RADIOASSAY KT
Applicant
Schwarz Mann
803 N. Front St. Suite 3
Mchenry,  IL  60050
Correspondent
Schwarz Mann
803 N. Front St. Suite 3
Mchenry,  IL  60050
Regulation Number862.1810
Classification Product Code
CDD  
Date Received11/01/1976
Decision Date 12/21/1976
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Clinical Chemistry
510k Review Panel Clinical Chemistry
Type Traditional
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
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