FDA 510(k), K811818, UROPAPER EIKEN UAG

FDA 510(k), K811818, UROPAPER EIKEN UAG

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510(K) Number: K811818
Device Name: UROPAPER EIKEN UAG
Manufacturer: SYN-KIT, INC.
Device Classification Name: method, enzymatic, glucose (urinary, non-quantitative)
Regulation Number: 862.1340
Classification Product Code: JIL
Date Received: 06/26/1981
Decision Date: 07/23/1981
Regulation Medical Specialty: Clinical Chemistry
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