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FDA 510(k), K904685, EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y)
FDA 510(k), K904685, EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y)
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510(K) Number: K904685
Device Name: EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y)
Manufacturer: HAMID
Device Classification Name: Set, Administration, Intravascular
Regulation Number: FPA
Classification Product Code: 10/04/1990
Date Received: 11/21/1990
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: EXEL HUBER INFUSION SET WITHOUT INJECTION SITE (Y)
Manufacturer: HAMID
Device Classification Name: Set, Administration, Intravascular
Regulation Number: FPA
Classification Product Code: 10/04/1990
Date Received: 11/21/1990
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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