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Deseret Multilumen Subclavian Jugular

by Parke-Davis Co. 2 variants

510(k) K840183

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 NumberK840183 Date19 Mar 1984ClearedStatusActive

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  • Withdrawn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
FOZ
Device Class
Class II
Regulation
21 CFR Part 880.5200
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 21 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 Desert Multilumen Subclavian Jugular is a multilumen catheter designed for subclavian and jugular vein access. It is intended for vascular access procedures requiring multiple lumens for administration of fluids or medications.

This device is supplied as a single-use product and requires appropriate storage conditions. It has received FDA 510(k) clearance with the product code FOZ and is manufactured by Parke-Davis Co. in Brookville, Ontario, Canada.

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