FDA 510(k), K032203, HEMOCUE HEMOGLOBIN 201 + SYSTEM ARTICLE 121704

FDA 510(k), K032203, HEMOCUE HEMOGLOBIN 201 + SYSTEM ARTICLE 121704

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510(K) Number: K032203
Device Name: HEMOCUE HEMOGLOBIN 201 + SYSTEM ARTICLE 121704
Manufacturer:
Device Classification Name: System, Hemoglobin, Automated
Regulation Number: 864.5620
Classification Product Code: GKR
Date Received: 07/18/2003
Decision Date: 08/25/2003
Regulation Medical Specialty: Hematology
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