Vapro Intermittent Catheter, Model 72062, 72082, 72102, 72122, 72142, 72064, 72084, 72104, 72124, 72144, 72164, 72184,

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K090960 ↗

FDA Product Code

GBM

Models / Variants

72062

72082

72102

72122

72142

72064

72084

72104

72124

72144

72164

72184

Device Class

Class II

Regulation

21 CFR Part 876.5130

Advisory Committee

Gastroenterology, Urology

FDA Decision

SESE Substantially Equivalent

• Incare Intermittent Catheter

  Class II

  FDA 510(k) K013345 Active Cleared 7 Jan 2002

• Heelbo Quilted Torso Restraint

  Class I

  FDA 510(k) K963108 Active Cleared 9 Oct 1996

• Incare Pressure Biofeedback Vaginal Pressure Probe and Anal Pressure Probe

  Class II

  FDA 510(k) K013653 Active Cleared 5 Mar 2002

• Incare Pinsite Dressing

  Class I

  FDA 510(k) K905206 Active Cleared 12 Apr 1991

• Checkmate Ankle Restraint System

  Class I

  FDA 510(k) K962963 Active Cleared 24 Oct 1996

• Microgyn II Elec Stim Device Treat of Urin Inconti

  Class II

  FDA 510(k) K891773 Active Cleared 23 Aug 1989

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