Braided High Pressure Catheter Connector

FDA 510(k) K905415 · The R Group

Substantially Equivalent

510(k) numberK905415

Submission

Device name
Braided High Pressure Catheter Connector
Applicant
The R Group
Gainesvilles, FL, US
Received
December 4, 1990
Decision date
August 12, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FOZ – Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5200
Specialty
General Hospital

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K260432Ruby Intravascular CatheterFOZ · Traditional Venocare, Inc.09/02/2026SE
K260165Unimpregnated Central Venous CatheterFOZ · Traditional Spectrum Vascular08/10/2026SE
K261041ClearSafe Closed SystemFOZ · Traditional MedSource Labs, LLC07/10/2026SE
K260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterFOZ · Traditional MedSource Labs, LLC07/09/2026SE
K253235Introcan Safety® Deep Access XL IV CatheterFOZ · Traditional B.Braun Medical, Inc.05/15/2026SE
K252137BD Insyte™ IV CatheterFOZ · Traditional Becton Dickinson Infusion Therapy Systems, Inc.04/02/2026SE
K252513Polywin Safety (14G x 51mm; 16G x 51mm; 18G x 64mm; 20G x 64mm; 20G x 45mm; 22G x 64mm…FOZ · Special Poly Medicure Limited04/01/2026SE
K252398SURFLO Hybria Closed System Safety IV CatheterFOZ · Traditional Terumo Medical Products (Hangzhou) Co., Ltd.12/17/2025SE
K252677Polyshield Safety IV CathetersFOZ · Special Poly Medicure Limited11/05/2025SE
K251422BD Saf-T-Intima™ Subcutaneous Catheter SystemFOZ · Traditional Becton Dickinson Infusion Therapy Systems, Inc.10/08/2025SE

More from Becton Dickinson Infusion Therapy Systems, Inc.

510(k)DeviceDecision
K912076Poly Braided Pigtail/Perc Card Cath W/Var Tip ConfDQO · Traditional 07/30/1991SE
K911549Injector Fill TubeDXT · Traditional 07/18/1991SE
K905416Vessel DilatorDRE · Traditional 03/25/1991SE

Questions and answers

When was Braided High Pressure Catheter Connector cleared by the FDA?

Braided High Pressure Catheter Connector (K905415) received a 510(k) decision of Substantially Equivalent on August 12, 1991, 251 days after the submission was received.

What is the product code of K905415?

The FDA product code is FOZ – Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days, a Class II (moderate risk) device regulated under 21 CFR 880.5200.