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FDA 510(k), K971509, ENDOXANE
FDA 510(k), K971509, ENDOXANE
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510(K) Number: K971509
Device Name: ENDOXANE
Manufacturer: BRUNO FERREYROL
Device Classification Name: Prosthesis, Tracheal, Preformed/Molded
Regulation Number: NWA
Classification Product Code: 04/25/1997
Date Received: 08/21/1997
Decision Date: SE SUBJECT TO TRACKING REG (ST)
Regulation Medical Specialty: General & Plastic Surgery
Device Name: ENDOXANE
Manufacturer: BRUNO FERREYROL
Device Classification Name: Prosthesis, Tracheal, Preformed/Molded
Regulation Number: NWA
Classification Product Code: 04/25/1997
Date Received: 08/21/1997
Decision Date: SE SUBJECT TO TRACKING REG (ST)
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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