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FDA 510(k), K012879, EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITE
FDA 510(k), K012879, EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITE
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510(K) Number: K012879
Device Name: EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITE
Manufacturer: ARMAND HAMID
Device Classification Name: Set, Administration, Intravascular
Regulation Number: FPA
Classification Product Code: 08/28/2001
Date Received: 01/17/2002
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: EXEL HUBER INFUSION SET WITH NEEDLELESS INJECTION SITE
Manufacturer: ARMAND HAMID
Device Classification Name: Set, Administration, Intravascular
Regulation Number: FPA
Classification Product Code: 08/28/2001
Date Received: 01/17/2002
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
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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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