FDA 510(k), K122337, OVUSENSE
FDA 510(k), K122337, OVUSENSE
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$149.00 USD
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510(K) Number: K122337
Device Name: OVUSENSE
Manufacturer:
Device Classification Name: Device, Fertility Diagnostic, Proceptive
Regulation Number:
Classification Product Code: LHD
Date Received: 08/02/2012
Decision Date: 08/06/2013
Regulation Medical Specialty:
Device Name: OVUSENSE
Manufacturer:
Device Classification Name: Device, Fertility Diagnostic, Proceptive
Regulation Number:
Classification Product Code: LHD
Date Received: 08/02/2012
Decision Date: 08/06/2013
Regulation Medical Specialty: