Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

KISH URETHRAL ILLUMINATED CATHETER SET

K-Number: K810367 · 1981-03-20

ApplicantVance Products, Inc.
Decision Date1981-03-20
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KISH URETHRAL ILLUMINATED CATHETER SET is the device name listed in this FDA 510(k) record. The listed applicant is Vance Products, Inc.. It received FDA 510(k) clearance on 1981-03-20 under 510(k) number K810367. 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 KISH URETHRAL ILLUMINATED CATHETER SET?

KISH URETHRAL ILLUMINATED CATHETER SET is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Vance Products, Inc.. The 510(k) number is K810367.

When did KISH URETHRAL ILLUMINATED CATHETER SET receive FDA 510(k) clearance?

KISH URETHRAL ILLUMINATED CATHETER SET received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810367.

Who is the listed applicant for KISH URETHRAL ILLUMINATED CATHETER SET?

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

What is the FDA product code for KISH URETHRAL ILLUMINATED CATHETER SET?

The FDA product code for KISH URETHRAL ILLUMINATED CATHETER SET 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Vance Products, 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.

K820313VPI-FAIR URETHRAL STENTK812995VANCE-JACOBELLIS MICROHEMATURIA CATHETERK813278VPI URETERAL DILATATION BALLON CATHETERK812785VANCE-AMBROSE RESECTOSCOPE FORCEPSK812057VANCE CYSTOSCOPICK811833VNACE FASCIAL DILATOR SET

View all 17 devices →

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.

↑