FDA 510(k), K932363, UROPAPER EIKEN GK

FDA 510(k), K932363, UROPAPER EIKEN GK

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510(K) Number: K932363
Device Name: UROPAPER EIKEN GK
Manufacturer: TANABE U.S.A., INC.
Device Classification Name: method, enzymatic, glucose (urinary, non-quantitative)
Regulation Number: 862.1340
Classification Product Code: JIL
Date Received: 04/19/1993
Decision Date: 11/16/1993
Regulation Medical Specialty: Clinical Chemistry
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