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FDA 510(k)

URINARY DIVERSION STENT

K-Number: K830803 · 1983-05-05

ApplicantVan-Tec, Inc.
Decision Date1983-05-05
Product CodeLJE
DecisionSubstantially Equivalent

Device Summary

URINARY DIVERSION STENT is the device name listed in this FDA 510(k) record. The listed applicant is Van-Tec, Inc.. It received FDA 510(k) clearance on 1983-05-05 under 510(k) number K830803. The device is classified under product code LJE. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the URINARY DIVERSION STENT?

URINARY DIVERSION STENT is a medical device that received FDA 510(k) clearance on 1983-05-05. The listed applicant is Van-Tec, Inc.. The 510(k) number is K830803.

When did URINARY DIVERSION STENT receive FDA 510(k) clearance?

URINARY DIVERSION STENT received FDA 510(k) clearance on 1983-05-05, under 510(k) number K830803.

Who is the listed applicant for URINARY DIVERSION STENT?

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

What is the FDA product code for URINARY DIVERSION STENT?

The FDA product code for URINARY DIVERSION STENT is LJE.

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Other records listing Van-Tec, Inc. as applicant

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Related Devices (Code: LJE)

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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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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