Exel Indwelling Catheter

No FDA recalls on record, checked 11 Oct 2026.

510(k) Number

K895772 ↗

FDA Product Code

FDZ

Device Class

Class I

Regulation

21 CFR Part 876.1500

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 a-V Fistula Set

  Class II

  FDA 510(k) K903945 Active Cleared 20 Nov 1990

See all devices from Exel Intl. →