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FDA 510(k), K040163, MICROVASCULAR ANASTOMOTIC DEVICE
FDA 510(k), K040163, MICROVASCULAR ANASTOMOTIC DEVICE
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510(K) Number: K040163
Device Name: MICROVASCULAR ANASTOMOTIC DEVICE
Manufacturer: DAISY P SIN
Device Classification Name: Device, Anastomotic, Microvascular
Regulation Number: MVR
Classification Product Code: 01/26/2004
Date Received: 04/16/2004
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: MICROVASCULAR ANASTOMOTIC DEVICE
Manufacturer: DAISY P SIN
Device Classification Name: Device, Anastomotic, Microvascular
Regulation Number: MVR
Classification Product Code: 01/26/2004
Date Received: 04/16/2004
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General & Plastic Surgery
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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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