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FDA 510(k), K981645, TITANIUM HEMOSTATIC CLIP
FDA 510(k), K981645, TITANIUM HEMOSTATIC CLIP
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510(K) Number: K981645
Device Name: TITANIUM HEMOSTATIC CLIP
Manufacturer: VITALITEC INT'L., INC.
Device Classification Name: clip, implantable
Regulation Number: 878.4300
Classification Product Code: FZP
Date Received: 05/08/1998
Decision Date: 10/13/1998
Regulation Medical Specialty: General & Plastic Surgery
Device Name: TITANIUM HEMOSTATIC CLIP
Manufacturer: VITALITEC INT'L., INC.
Device Classification Name: clip, implantable
Regulation Number: 878.4300
Classification Product Code: FZP
Date Received: 05/08/1998
Decision Date: 10/13/1998
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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