Bardex I.C. Latex Foley Catheter

FDA 510(k) K040658 · C.R. Bard, Inc.

Substantially Equivalent

510(k) numberK040658

Submission

Device name
Bardex I.C. Latex Foley Catheter
Applicant
C.R. Bard, Inc.
Covington, GA, US
Received
March 12, 2004
Decision date
September 29, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MJC – Catheter, Urological (Antimicrobial) And Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5130
Specialty
Gastroenterology, Urology

Other 510(k)s with product code MJC

510(k)DeviceApplicantDecision
K233094Wellead® Latex Foley CatheterMJC · Traditional Well Lead Medical (Hainan) Co., Ltd.06/06/2024SE
K033477Hydrophilic-Antibacterial Intermittent Catheter, Intermittent Catheter Closed System KitMJC · Traditional Rochester Medical Corp.06/10/2004SE
K000251Spectrum Silicone Foley CatheterMJC · Traditional Cook Urological, Inc.08/30/2000SE
K001143Release NF Antibacterial Foley Catheter, Antibacterial Personal CatheterMJC · Traditional Rochester Medical Corp.07/07/2000SE
K993464Bardex I.C. Pediatric Foley CatheterMJC · Abbreviated C.R. Bard, Inc.12/10/1999SE
K984136Bardex Lubri-Sil I.C. Foley CatheterMJC · Traditional Bard Medical Div.02/16/1999SE
K983101Bardex I.C 4-WAY Foley Catheter Model 1865SIXX XX = 18,20,22,24MJC · Abbreviated C.R. Bard, Inc.11/03/1998SE
K971627Silicone Antibacterial Foley CatheterMJC · Traditional Rochester Medical Corp.01/13/1998SE
K910318Bard(R) Hydrogel/Silver-Coated Foley CatheterMJC · Traditional C.R. Bard, Inc.08/18/1994SE

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Questions and answers

When was Bardex I.C. Latex Foley Catheter cleared by the FDA?

Bardex I.C. Latex Foley Catheter (K040658) received a 510(k) decision of Substantially Equivalent on September 29, 2004, 201 days after the submission was received.

What is the product code of K040658?

The FDA product code is MJC – Catheter, Urological (Antimicrobial) And Accessories, a Class II (moderate risk) device regulated under 21 CFR 876.5130.