Skip to content

Curity & Kenguard Silicone Coated Foley Catheter

by The Kendal Co.

510(k) K860484

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

1 ongoing

This device is named in the recall

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK860484 Date11 Mar 1986ClearedStatusActive

Recalls

1 recall · 1 ongoing · FDA

    • Ongoing Z-1052-2024 FDA Class I initiated 4 Dec 2023

    Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
KOD
Device Class
Class II
Regulation
21 CFR Part 876.5130
Advisory Committee
Gastroenterology, Urology
FDA Decision
SESE Substantially Equivalent

Other devices from The Kendal Co.

See all devices from The Kendal Co. →