FDA 510(k), K894949, SQA

FDA 510(k), K894949, SQA

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510(K) Number: K894949
Device Name: SQA
Manufacturer:
Device Classification Name: Semen Analysis Device
Regulation Number: 864.5220
Classification Product Code: POV
Date Received: 08/03/1989
Decision Date: 12/29/1989
Regulation Medical Specialty: Hematology
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