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FDA 510(k)

TOUCHLESS CLEAN-CATH

K-Number: K802665 · 1980-11-12

ApplicantDiamed Division Ill. Tool Works, Inc.
Decision Date1980-11-12
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TOUCHLESS CLEAN-CATH is the device name listed in this FDA 510(k) record. The listed applicant is Diamed Division Ill. Tool Works, Inc.. It received FDA 510(k) clearance on 1980-11-12 under 510(k) number K802665. 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 TOUCHLESS CLEAN-CATH?

TOUCHLESS CLEAN-CATH is a medical device that received FDA 510(k) clearance on 1980-11-12. The listed applicant is Diamed Division Ill. Tool Works, Inc.. The 510(k) number is K802665.

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

TOUCHLESS CLEAN-CATH received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802665.

Who is the listed applicant for TOUCHLESS CLEAN-CATH?

The FDA 510(k) record lists Diamed Division Ill. Tool Works, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TOUCHLESS CLEAN-CATH?

The FDA product code for TOUCHLESS CLEAN-CATH is KOD.

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Other records listing Diamed Division Ill. Tool Works, 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.

K854953DIAMED MODELS 600, 900, 960, 964K823450FEMALE EXTERNAL URINARY APPLIANCEK812281TOUCHLESS HOME-CATHK802664URINARY DRAINAGE UNTK790728TOUCHLESS TM FOLEY CATHETER KITK760897STERILE URETHRAL CATHETER KIT

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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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