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FDA 510(k)

CATH-SECURE

K-Number: K803062 · 1981-01-07

ApplicantMelissa C. Johnson
Decision Date1981-01-07
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATH-SECURE is the device name listed in this FDA 510(k) record. The listed applicant is Melissa C. Johnson. It received FDA 510(k) clearance on 1981-01-07 under 510(k) number K803062. 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 CATH-SECURE?

CATH-SECURE is a medical device that received FDA 510(k) clearance on 1981-01-07. The listed applicant is Melissa C. Johnson. The 510(k) number is K803062.

When did CATH-SECURE receive FDA 510(k) clearance?

CATH-SECURE received FDA 510(k) clearance on 1981-01-07, under 510(k) number K803062.

Who is the listed applicant for CATH-SECURE?

The FDA 510(k) record lists Melissa C. Johnson as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATH-SECURE?

The FDA product code for CATH-SECURE is KOD.

Related Clinical Trials

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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

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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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