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FDA 510(k), K051814, JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET
FDA 510(k), K051814, JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET
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510(K) Number: K051814
Device Name: JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET
Manufacturer: JMS NORTH AMERICA CORP.
Device Classification Name: Needle, Fistula
Regulation Number: 876.5540
Classification Product Code: FIE
Date Received: 07/05/2005
Decision Date: 08/04/2005
Regulation Medical Specialty: Gastroenterology/Urology
Device Name: JMS SYSLOC MINI A.V. FISTULA NEEDLE SET AND APHERESIS NEEDLE SET
Manufacturer: JMS NORTH AMERICA CORP.
Device Classification Name: Needle, Fistula
Regulation Number: 876.5540
Classification Product Code: FIE
Date Received: 07/05/2005
Decision Date: 08/04/2005
Regulation Medical Specialty: Gastroenterology/Urology
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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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