Kendall Curity Suprapubic Catheter Tray, Kit, & Replacement Set

No FDA recalls found in the data synced 9 Oct 2026.

510(k) Number

K970969 ↗

FDA Product Code

KOB

Device Class

Class II

Regulation

21 CFR Part 876.5090

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Curity Venous Catheterization Kit

  Class II

  FDA 510(k) K861828 Active Cleared 10 Jul 1986

• Curity Fiberoptic Intubating Airway

  Class I

  FDA 510(k) K855137 Active Cleared 11 Mar 1986

• Curity Curad Bandages

  Class I

  FDA 510(k) K810126 Active Cleared 6 Feb 1981

• The Kendall Urinary Output Monitor

  Class I

  FDA 510(k) K852083 Active Cleared 20 Sep 1985

• Kendall Curity Irrigation Syringe

  Class II

  FDA 510(k) K892436 Active Cleared 14 Jul 1989

• Curity Continuous Epidural Anesthesia Tray

  Class II

  FDA 510(k) K871066 Active Cleared 15 May 1987

See all devices from The Kendal Co. →