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Stopcock 196590

by Argon Medical Devices, Inc.

Stopcock 196590 is a Class II device made by Argon Medical Devices, Inc., cleared under FDA 510(k) K915301 on 11 Dec 1992 and listed in FDA GUDID since 20 Sep 2016 (UDI-DI 00886333208661), active as of 22 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 22 Oct 2026

Documents

510(k) K915301

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00886333208661 UDI-DI Date20 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK915301 Date11 Dec 1992DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K915301 decided 11 Dec 1992 Active
  • FDA GUDID UDI-DI 00886333208661 listed 20 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K915301
  2. Listed FDA GUDID 00886333208661

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Stopcock
Generic name
Intravenous line stopcock
Model / Ref / Catalog
196590
Primary DI / UDI-DI
00886333208661
510(k) Number
FDA product code
DTL
GMDN term
Intravenous line stopcock
Device class
Class II
Regulation number
870.4290
GUDID distribution status
In Commercial Distribution

Similar devices in this category

Other devices filed under Intravenous line stopcock.

Other devices from Argon Medical Devices, Inc.

See all devices from Argon Medical Devices, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)