FDA 510(k), K843532, UROPAPER EIKEN 8

FDA 510(k), K843532, UROPAPER EIKEN 8

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510(K) Number: K843532
Device Name: UROPAPER EIKEN 8
Manufacturer:
Device Classification Name: Reagent, Occult Blood
Regulation Number: 864.6550
Classification Product Code: KHE
Date Received: 09/07/1984
Decision Date: 12/12/1984
Regulation Medical Specialty: Hematology
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