FDA 510(k), K932367, UROPAPER EIKEN 8

FDA 510(k), K932367, UROPAPER EIKEN 8

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510(K) Number: K932367
Device Name: UROPAPER EIKEN 8
Manufacturer:
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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