Exel a-V Fistula Set

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K903945 ↗

FDA Product Code

FIE

Device Class

Class II

Regulation

21 CFR Part 876.5540

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Exel Spinal Needles

  Class II

  FDA 510(k) K895771 Active Cleared 16 Feb 1990

• Exel Dental Needle

  Class I

  FDA 510(k) K861150 Active Cleared 11 Apr 1986

• Exel Huber Infusion Set Rotating Wing

  Class II

  FDA 510(k) K926119 Active Cleared 11 Aug 1993

• Exel Safelet Catheter

  Class II

  FDA 510(k) K895768 Active Cleared 16 Feb 1990

• Disposable Syringes and Hypodermic Needles

  Class II

  FDA 510(k) K861153 Active Cleared 23 Apr 1986

• Exel Avf Single Needle

  Class II

  FDA 510(k) K963658 Active Cleared 5 May 1998

See all devices from Exel Intl. →