FDA 510(k), K990184, AUTOMARQER

FDA 510(k), K990184, AUTOMARQER

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510(K) Number: K990184
Device Name: AUTOMARQER
Manufacturer:
Device Classification Name: Semen Analysis Device
Regulation Number: 864.5220
Classification Product Code: POV
Date Received: 01/20/1999
Decision Date: 03/19/1999
Regulation Medical Specialty: Hematology
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