Skip to content

VPS Catheter

by Vasonova, Inc.

510(k) K091924

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 NumberK091924 Date18 Nov 2009ClearedStatusActive

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  • Withdrawn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
LJS
Device Class
Class II
Regulation
21 CFR Part 880.5970
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 24 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 VPS Catheter is an intravascular catheter designed for therapeutic use over long periods greater than 30 days. It is classified under product code LJS and is intended for general hospital applications.

The device is supplied by Vasonova, Inc. and received FDA 510(k) clearance on November 18, 2009, with a decision code of SESE. It is a Class II device under regulation number 880.5970 and is not a third-party reviewed product.

Other devices from Vasonova, Inc.

See all devices from Vasonova, Inc. →