Vitalcare Urethral Catheter

FDA 510(k) K021938 · Vitalcare, Inc.

Substantially Equivalent

510(k) numberK021938

Submission

Device name
Vitalcare Urethral Catheter
Applicant
Vitalcare, Inc.
Miami, FL, US
Received
June 12, 2002
Decision date
April 22, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GBM – Catheter, Urethral
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5130
Specialty
Gastroenterology, Urology

Other 510(k)s with product code GBM

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K241734Wellead® Hydrophilic Intermittent Catheter Ready to Use; Wellead® Hydrophilic…GBM · Traditional Well Lead Medical Co., Ltd.03/05/2025SE
K213283GentleCath Air for Men Hydrophilic Intermittent Urinary CatheterGBM · Traditional Convatec Limited06/22/2022SE
K211436Intermittent Catheter (Not Finalized)GBM · Traditional Hollister Incorporated01/27/2022SE
K200820SpeediCath Compact SetGBM · Traditional Coloplast11/13/2020SE
K192904SpeediCath Compact SetGBM · Traditional Coloplast11/02/2020SE
K200142SpeediCath SoftGBM · Traditional Coloplast07/30/2020SE
K200134Jimushi Sterile Urethral Catheter for single useGBM · Traditional Hangzhou Jimushi Meditech Co., Ltd.06/01/2020SE
K191512LotusCatheter (Lotus No Balloon Catheter)GBM · Traditional Hakki Medical Technologies, Inc.05/21/2020SESK
K192577Actreen Hi-Lite Intermittent Urinary CathetersGBM · Special B.Braun Medical, Inc.05/07/2020SE
K193148VaPro Plus Pocket, VaPro PlusGBM · Special Hollister Incorporated12/13/2019SE

More from Hollister Incorporated

510(k)DeviceDecision
K021939Vitalcare Foley CatheterEZL · Traditional 04/22/2003SE
K023872Vitalcare Urethral Catheter Red RubberEZD · Traditional 04/10/2003SE

Questions and answers

When was Vitalcare Urethral Catheter cleared by the FDA?

Vitalcare Urethral Catheter (K021938) received a 510(k) decision of Substantially Equivalent on April 22, 2003, 314 days after the submission was received.

What is the product code of K021938?

The FDA product code is GBM – Catheter, Urethral, a Class II (moderate risk) device regulated under 21 CFR 876.5130.