Skip to content

Winged Non-Coring Needle Set

by Marquette Medical, Inc.

510(k) K884212

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 NumberK884212 Date17 Oct 1988ClearedStatusActive

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  • Withdrawn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
FMI
Device Class
Class II
Regulation
21 CFR Part 880.5570
Advisory Committee
General Hospital
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 6 Oct 2026

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

This device is a winged non-coring needle set, a Class 2 general hospital device with product code FMI. It is substantially equivalent to a predicate device and was cleared through the traditional 510(k) pathway.

It is manufactured by Marquette Medical, Inc., received FDA 510(k) clearance under K884212 on October 17, 1988, following a 11-day review. The device is supplied as a finished product and is intended for use in general hospital settings.

Other devices from Marquette Medical, Inc.

See all devices from Marquette Medical, Inc. →