Skip to content

Curity Venous Catheterization Kit

by The Kendal Co.

510(k) K861828

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

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 NumberK861828 Date10 Jul 1986ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

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  • Withdrawn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
DQY
Device Class
Class II
Regulation
21 CFR Part 870.1250
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 27 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Curity Venous Catheterization Kit is designed to facilitate venous access for therapeutic or diagnostic purposes. It typically includes a catheter, needle, and other components necessary for safe and effective venous catheterization. This device is crucial in settings where intravenous access is needed, such as administering medications, fluids, or obtaining blood samples.

The Curity Venous Catheterization Kit is supplied as a complete kit for venous catheterization procedures. It is regulated under product code DQY and received FDA 510(k) clearance with number K861828 on July 10, 1986, as substantially equivalent to predicate devices.

Other devices from The Kendal Co.

See all devices from The Kendal Co. →