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FDA 510(k)

CONVEEN INTERMITTENT CATHETERS

K-Number: K895548 · 1990-02-09

ApplicantColoplast A/S
Decision Date1990-02-09
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CONVEEN INTERMITTENT CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Coloplast A/S. It received FDA 510(k) clearance on 1990-02-09 under 510(k) number K895548. The device is classified under product code KOD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVEEN INTERMITTENT CATHETERS?

CONVEEN INTERMITTENT CATHETERS is a medical device that received FDA 510(k) clearance on 1990-02-09. The listed applicant is Coloplast A/S. The 510(k) number is K895548.

When did CONVEEN INTERMITTENT CATHETERS receive FDA 510(k) clearance?

CONVEEN INTERMITTENT CATHETERS received FDA 510(k) clearance on 1990-02-09, under 510(k) number K895548.

Who is the listed applicant for CONVEEN INTERMITTENT CATHETERS?

The FDA 510(k) record lists Coloplast A/S as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONVEEN INTERMITTENT CATHETERS?

The FDA product code for CONVEEN INTERMITTENT CATHETERS is KOD.

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Other records listing Coloplast A/S as applicant

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Related Devices (Code: KOD)

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.

K251864Rubber Utility CatheterC.R. Bard, Inc.K220036Wellead Ureteral CatheterWell Lead Medical Co., Ltd.K220730allFlex Ureteral Catheters, Krait Ureteral CathetersAllwin Medical Devices, Inc.K211032Urinary Catheter 12 Fr, Urinary Catheter 16 FrUrogen Pharma, Ltd.K181979Rusch FloCath Quick 18 Fr. Coudé Hydrophilic Intermittent CatheterTeleflexmedical, Inc.K180354UroGen Ureteral CatheterUrogen Pharma, Ltd.

Official Source

View on FDA Database →

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

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