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

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