Arrow Brachial Central Venous Cath-Kit W/16GA & Ec

FDA 510(k) K854137 · Arrow Intl., Inc.

Substantially Equivalent

510(k) numberK854137

Submission

Device name
Arrow Brachial Central Venous Cath-Kit W/16GA & Ec
Applicant
Arrow Intl., Inc.
Reading, PA, US
Received
October 10, 1985
Decision date
December 3, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DQY – Catheter, Percutaneous
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1250
Specialty
Cardiovascular

Other 510(k)s with product code DQY

510(k)DeviceApplicantDecision
K260559NHanceITDQY · Traditional IMDS Operation B.V.08/14/2026SE
K262392APRO 35 Swift CatheterDQY · Special Alembic, LLC08/12/2026SE
K262240SSPC NXT Delivery CatheterDQY · Special CenterPoint Systems, LLC07/29/2026SE
K261766CPS Locator 3D Plus Delivery CatheterDQY · Special CenterPoint Systems, LLC07/29/2026SE
K261825Amplatzer TorqVue LP Delivery System; Amplatzer TorqVue LP CatheterDQY · Special Abbott07/02/2026SE
K261631Amplatzer TorqVue Exchange SystemDQY · Special Abbott Medical06/17/2026SE
K260289Perfect-O Ostial Positioning CatheterDQY · Traditional Balosmark, Inc.06/05/2026SE
K260993Amplatzer TorqVue Delivery SystemDQY · Special Abbott04/24/2026SE
K253361Teleport Glide MicrocatheterDQY · Traditional OrbusNeich Medical (Shenzhen) Co., Ltd.04/10/2026SE
K260499Amplatzer™ Trevisio™ Intravascular Delivery System; 9-ATV06F45/609-ATV07F45/609-ATV07F45/…DQY · Special Abbott Medical03/13/2026SE

More from Abbott Medical

510(k)DeviceDecision
K100635Arrowgard Evolution Antimicrobial Peripherally Inserted Central Catheter (Picc) Model:…LJS · Traditional 08/27/2010SE
K093050Arrow Seldinger Arterial Catherization Devices, Models Ex Sac 00520DQY · Special 12/18/2009SE
K071491Arrow International, Inc., Surgical DrapesKKX · Traditional 10/10/2007SE
K071998Arrow Echogenic Introducer Needle ComponentFMI · Special 09/26/2007SE
K071111Non-Absorbable Silk SutureGAP · Traditional 07/17/2007SE
K060309Autocat Intra-Aortic Balloon Pump SeriesDSP · Special 04/06/2006SE
K042126PiccLJS · Special 08/27/2004SESU
K041153Sharpsaway II Locking Disposable CupFMI · Traditional 07/12/2004SE
K040801Intra-Aortic Balloon (Iab)DSP · Special 05/06/2004SE
K040802Hemosonic 200HEMODYNAMIC MonitorDPN · Special 04/28/2004SE

Questions and answers

When was Arrow Brachial Central Venous Cath-Kit W/16GA & Ec cleared by the FDA?

Arrow Brachial Central Venous Cath-Kit W/16GA & Ec (K854137) received a 510(k) decision of Substantially Equivalent on December 3, 1985, 54 days after the submission was received.

What is the product code of K854137?

The FDA product code is DQY – Catheter, Percutaneous, a Class II (moderate risk) device regulated under 21 CFR 870.1250.