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FDA 510(k), K020189, EXEL BUTTERFLY SCALP VEIN SET
FDA 510(k), K020189, EXEL BUTTERFLY SCALP VEIN SET
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510(K) Number: K020189
Device Name: EXEL BUTTERFLY SCALP VEIN SET
Manufacturer: TAMMIE EWING
Device Classification Name: Set, Administration, Intravascular
Regulation Number: FPA
Classification Product Code: 01/18/2002
Date Received: 03/27/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: General Hospital
Device Name: EXEL BUTTERFLY SCALP VEIN SET
Manufacturer: TAMMIE EWING
Device Classification Name: Set, Administration, Intravascular
Regulation Number: FPA
Classification Product Code: 01/18/2002
Date Received: 03/27/2003
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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