Skip to content

Inrad 15423

by Inrad

Inrad 15423 is a Class I device made by Inrad, cleared under FDA 510(k) K896019 on 3 Jan 1990 and listed in FDA GUDID since 8 Oct 2026 (UDI-DI 00817295020008), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K896019

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817295020008 UDI-DI Date8 Oct 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK896019 Date3 Jan 1990DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K896019 decided 3 Jan 1990 Active
  • FDA GUDID UDI-DI 00817295020008 listed 8 Oct 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K896019
  2. Listed FDA GUDID 00817295020008

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Inrad
Generic name
Body aspiration needle, single-use
Model / Ref / Catalog
15423
Primary DI / UDI-DI
00817295020008
510(k) Number
FDA product code
GAA
GMDN term
Body aspiration needle, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GAA (Needle, Aspiration And Injection, Disposable).

Other devices from Inrad

  • Inrad 53220

    Class I
  • Inrad 53222

    Class I
  • Inrad 53218

    Class I
  • Inrad 41222

    Class I

See all devices from Inrad →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (10, all answered No)