FDA 510(k), K980814, PURESPERM
FDA 510(k), K980814, PURESPERM
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510(K) Number: K980814
Device Name: PURESPERM
Manufacturer:
Device Classification Name: Media, Reproductive
Regulation Number: 884.6180
Classification Product Code: MQL
Date Received: 03/03/1998
Decision Date: 06/23/1998
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: PURESPERM
Manufacturer:
Device Classification Name: Media, Reproductive
Regulation Number: 884.6180
Classification Product Code: MQL
Date Received: 03/03/1998
Decision Date: 06/23/1998
Regulation Medical Specialty: Obstetrics/Gynecology