FDA 510(k), K980627, NEVA SYSTEM
FDA 510(k), K980627, NEVA SYSTEM
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510(K) Number: K980627
Device Name: NEVA SYSTEM
Manufacturer:
Device Classification Name: Monitor, Penile Tumescence
Regulation Number:
Classification Product Code: LIL
Date Received: 02/18/1998
Decision Date: 04/07/1998
Regulation Medical Specialty:
Device Name: NEVA SYSTEM
Manufacturer:
Device Classification Name: Monitor, Penile Tumescence
Regulation Number:
Classification Product Code: LIL
Date Received: 02/18/1998
Decision Date: 04/07/1998
Regulation Medical Specialty: