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FDA 510(k)

TELESCOPE PROTECTION TUBE

K-Number: K860265 · 1986-04-07

ApplicantR. J. Ltd., Ind.
Decision Date1986-04-07
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

TELESCOPE PROTECTION TUBE is the device name listed in this FDA 510(k) record. The listed applicant is R. J. Ltd., Ind.. It received FDA 510(k) clearance on 1986-04-07 under 510(k) number K860265. 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 TELESCOPE PROTECTION TUBE?

TELESCOPE PROTECTION TUBE is a medical device that received FDA 510(k) clearance on 1986-04-07. The listed applicant is R. J. Ltd., Ind.. The 510(k) number is K860265.

When did TELESCOPE PROTECTION TUBE receive FDA 510(k) clearance?

TELESCOPE PROTECTION TUBE received FDA 510(k) clearance on 1986-04-07, under 510(k) number K860265.

Who is the listed applicant for TELESCOPE PROTECTION TUBE?

The FDA 510(k) record lists R. J. Ltd., Ind. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TELESCOPE PROTECTION TUBE?

The FDA product code for TELESCOPE PROTECTION TUBE 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 R. J. Ltd., Ind. 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.

K860266ELLIK EVACUATOR

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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