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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: KXA
Date Received: 06/17/1999
Decision Date: 02/10/2000
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
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: KXA
Date Received: 06/17/1999
Decision Date: 02/10/2000
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Gastroenterology/Urology
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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