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FDA 510(k), K940982, ARTERIAL EMBOLIZATION DEVICE (KRD)
FDA 510(k), K940982, ARTERIAL EMBOLIZATION DEVICE (KRD)
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510(K) Number: K940982
Device Name: ARTERIAL EMBOLIZATION DEVICE (KRD)
Manufacturer: APRIL LAVENDER
Device Classification Name: Device, Vascular, For Promoting Embolization
Regulation Number: KRD
Classification Product Code: 03/01/1994
Date Received: 10/14/1994
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
Device Name: ARTERIAL EMBOLIZATION DEVICE (KRD)
Manufacturer: APRIL LAVENDER
Device Classification Name: Device, Vascular, For Promoting Embolization
Regulation Number: KRD
Classification Product Code: 03/01/1994
Date Received: 10/14/1994
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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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