510(k) K222279

Device
Rusch Intermittent Urethral Catheters
Applicant
Teleflex Medical
510(k) number
K222279
Product code
EZC
Decision
Substantially Equivalent (SESE)
Decision date
2022-08-29
Date received
2022-07-29
Regulation
876.5130
Classification name
Catheter, Coude
Medical specialty
Gastroenterology, Urology
Review panel
Gastroenterology, Urology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Kelly Breheim
Address
3015 Carrington Mill Blvd. Morrisville NC US 27560 27560

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code EZC

510(k)DeviceApplicantDecision date
K173596Rusch Intermittent Urethral CathetersTeleflex Medical2018-01-29
K946282UNIVERSAL URETHRAL CATHETERLouisville Laboratories, Inc.1995-03-31
K913341BARD(R) COUDE TIP TEMPERATURE SENSING CATHETERC.R. Bard, Inc.1992-01-27
K910846BARD LATEX URINARY CATHETERS DRAINS- DESIGNS MODIFC.R. Bard, Inc.1991-08-16
K910195BARD HYDROGEL-COATED FOLEY CATHETERSC.R. Bard, Inc.1991-08-09
K910197HYDROGEL-COATED URETHRAL CATHETERS AND DRAINSC.R. Bard, Inc.1991-08-09