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FDA 510(k)

CATHETER, NATURAL LATEX URETHRAL

K-Number: K760440 · 1976-10-20

ApplicantAkron Catheter, Inc.
Decision Date1976-10-20
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CATHETER, NATURAL LATEX URETHRAL is the device name listed in this FDA 510(k) record. The listed applicant is Akron Catheter, Inc.. It received FDA 510(k) clearance on 1976-10-20 under 510(k) number K760440. 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 CATHETER, NATURAL LATEX URETHRAL?

CATHETER, NATURAL LATEX URETHRAL is a medical device that received FDA 510(k) clearance on 1976-10-20. The listed applicant is Akron Catheter, Inc.. The 510(k) number is K760440.

When did CATHETER, NATURAL LATEX URETHRAL receive FDA 510(k) clearance?

CATHETER, NATURAL LATEX URETHRAL received FDA 510(k) clearance on 1976-10-20, under 510(k) number K760440.

Who is the listed applicant for CATHETER, NATURAL LATEX URETHRAL?

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

What is the FDA product code for CATHETER, NATURAL LATEX URETHRAL?

The FDA product code for CATHETER, NATURAL LATEX URETHRAL is KOD.

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 Akron Catheter, 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.

K864736AKRO-SIL PLUSK823428KELLY INFLATABLE T DRAIN

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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