Uro-Tex Male External Catheter

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K832450 ↗

FDA Product Code

KNX

Device Class

Class II

Regulation

21 CFR Part 876.5250

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Uro Tex Urinals

  Class I

  FDA 510(k) K901000 Active Cleared 26 Mar 1990

• Model 820 Top=trak

  Class I

  FDA 510(k) K873039 Active Cleared 11 Feb 1988

• Comfort Sheath Reusable Male External Catheter

  Class I

  FDA 510(k) K962384 Active Cleared 15 Jul 1996

• Cone Cath

  Class I

  FDA 510(k) K931156 Active Cleared 1 Jul 1993

• Comfort Cath Self Adhering Male External Catheter

  Class I

  FDA 510(k) K934266 Active Cleared 19 Apr 1994

• Comfort Cath Special Self Adhering Male External Catheter

  Class I

  FDA 510(k) K962413 Active Cleared 15 Jul 1996

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