FDA 510(k), K992039, EXEL I.V. BLOOD LINE SET

FDA 510(k), K992039, EXEL I.V. BLOOD LINE SET

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510(K) Number: K992039
Device Name: EXEL I.V. BLOOD LINE SET
Manufacturer: ARMAND HAMID
Device Classification Name: Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
Regulation Number: FJK
Classification Product Code: 06/17/1999
Date Received: 02/10/2000
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology

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