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FDA 510(k)

VANCE-JACOBELLIS MICROHEMATURIA CATHETER

K-Number: K812995 · 1982-03-01

ApplicantVance Products, Inc.
Decision Date1982-03-01
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VANCE-JACOBELLIS MICROHEMATURIA CATHETER 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 1982-03-01 under 510(k) number K812995. 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 VANCE-JACOBELLIS MICROHEMATURIA CATHETER?

VANCE-JACOBELLIS MICROHEMATURIA CATHETER is a medical device that received FDA 510(k) clearance on 1982-03-01. The listed applicant is Vance Products, Inc.. The 510(k) number is K812995.

When did VANCE-JACOBELLIS MICROHEMATURIA CATHETER receive FDA 510(k) clearance?

VANCE-JACOBELLIS MICROHEMATURIA CATHETER received FDA 510(k) clearance on 1982-03-01, under 510(k) number K812995.

Who is the listed applicant for VANCE-JACOBELLIS MICROHEMATURIA CATHETER?

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 VANCE-JACOBELLIS MICROHEMATURIA CATHETER?

The FDA product code for VANCE-JACOBELLIS MICROHEMATURIA CATHETER is KOD.

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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 STENTK813278VPI URETERAL DILATATION BALLON CATHETERK812785VANCE-AMBROSE RESECTOSCOPE FORCEPSK812057VANCE CYSTOSCOPICK811833VNACE FASCIAL DILATOR SETK811454VANCE PROSTATIC ASPIRATION SET

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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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