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FDA 510(k), K063227, CONCEIVEX CONCEPTION KIT
FDA 510(k), K063227, CONCEIVEX CONCEPTION KIT
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510(K) Number: K063227
Device Name: CONCEIVEX CONCEPTION KIT
Manufacturer: CONCEIVEX INC.
Device Classification Name: kit, conception-assist, home use
Regulation Number: 884.5250
Classification Product Code: OBB
Date Received: 10/24/2006
Decision Date: 03/14/2007
Regulation Medical Specialty: Obstetrics/Gynecology
Device Name: CONCEIVEX CONCEPTION KIT
Manufacturer: CONCEIVEX INC.
Device Classification Name: kit, conception-assist, home use
Regulation Number: 884.5250
Classification Product Code: OBB
Date Received: 10/24/2006
Decision Date: 03/14/2007
Regulation Medical Specialty: Obstetrics/Gynecology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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