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FDA 510(k)

VITALCARE URETHRAL CATHETER RED RUBBER

K-Number: K023872 · 2003-04-10

ApplicantVitalcare, Inc.
Decision Date2003-04-10
Product CodeEZD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VITALCARE URETHRAL CATHETER RED RUBBER is the device name listed in this FDA 510(k) record. The listed applicant is Vitalcare, Inc.. It received FDA 510(k) clearance on 2003-04-10 under 510(k) number K023872. The device is classified under product code EZD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITALCARE URETHRAL CATHETER RED RUBBER?

VITALCARE URETHRAL CATHETER RED RUBBER is a medical device that received FDA 510(k) clearance on 2003-04-10. The listed applicant is Vitalcare, Inc.. The 510(k) number is K023872.

When did VITALCARE URETHRAL CATHETER RED RUBBER receive FDA 510(k) clearance?

VITALCARE URETHRAL CATHETER RED RUBBER received FDA 510(k) clearance on 2003-04-10, under 510(k) number K023872.

Who is the listed applicant for VITALCARE URETHRAL CATHETER RED RUBBER?

The FDA 510(k) record lists Vitalcare, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITALCARE URETHRAL CATHETER RED RUBBER?

The FDA product code for VITALCARE URETHRAL CATHETER RED RUBBER is EZD.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Vitalcare, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K021938VITALCARE URETHRAL CATHETERK021939VITALCARE FOLEY CATHETER

Related Devices (Code: EZD)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261418Liquick X-treme, Liquick X-treme PlusTeleflex MedicalK260737Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Female (CH06 - CH16); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Straight (CH06 - CH18); Cure Aqua™ Ready to Use Hydrophilic Intermittent Catheter Male Coude (CH10 - CH18).ConvatecK261658LoFric Origo Pro CoudéWellspect ABK262045Luja SoftColoplast A.S.K260394Hydrophilic coated intermittent nalaton catheter for single use-ready to use (NCR)Hangzhou Jimushi Meditech Co., Ltd.K253295Coude Sleeved IC; Coude Plus Sleeved ICHollister Incorporated

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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