Skip to content

Stockert V172-28 Venous Femoral Cannula

by Stockert Instrumente GmbH

510(k) K022321

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 NumberK022321 Date9 Oct 2002ClearedStatusActive

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  • Withdrawn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
DWF
Device Class
Class II
Regulation
21 CFR Part 870.4210
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 22 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 Stockert V172-28 Venous Femoral Cannula is a catheter, cannula and tubing device used for femoral vessel cannulation during cardiopulmonary bypass. It is designed for cannulation of the inferior vena cava and the right atrium via femoral access. The device features a wire-reinforced PVC cannula with a non-wire reinforced proximal end and two sets of side holes for drainage.

The Stockert V172-28 Venous Femoral Cannula is a sterile, single-use device with a size of 28 Fr and a length of 90 cm. It is supplied with an obturator to seal side holes. The device is regulated under FDA product code DWF and has a clearance type of Traditional, with an FDA 510(k) authorization.

Other devices from Stockert Instrumente GmbH

See all devices from Stockert Instrumente GmbH →

Questions

AI-generated answers, 22 Sep 2026

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

  • What is the Stockert V172-28 Venous Femoral Cannula used for?

    The Stockert V172-28 Venous Femoral Cannula is used for femoral vessel cannulation during cardiopulmonary bypass, specifically for cannulation of the inferior vena cava and the right atrium via femoral access.

  • Is the Stockert V172-28 Venous Femoral Cannula sterile and single-use?

    Yes, the Stockert V172-28 Venous Femoral Cannula is a sterile, single-use device, supplied with an obturator to seal side holes.

  • What are the size and length of the Stockert V172-28 Venous Femoral Cannula?

    The Stockert V172-28 Venous Femoral Cannula has a size of 28 Fr and a length of 90 cm.

  • What is the regulatory classification of the Stockert V172-28 Venous Femoral Cannula?

    The Stockert V172-28 Venous Femoral Cannula is regulated under FDA product code DWF, with a clearance type of Traditional and an FDA 510(k) authorization.