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FDA 510(k)

URETERAL CATHETER CONNECTOR

K-Number: K820868 · 1982-04-26

ApplicantVan-Tec, Inc.
Decision Date1982-04-26
Product CodeKOD
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

URETERAL CATHETER CONNECTOR 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 1982-04-26 under 510(k) number K820868. 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 URETERAL CATHETER CONNECTOR?

URETERAL CATHETER CONNECTOR is a medical device that received FDA 510(k) clearance on 1982-04-26. The listed applicant is Van-Tec, Inc.. The 510(k) number is K820868.

When did URETERAL CATHETER CONNECTOR receive FDA 510(k) clearance?

URETERAL CATHETER CONNECTOR received FDA 510(k) clearance on 1982-04-26, under 510(k) number K820868.

Who is the listed applicant for URETERAL CATHETER CONNECTOR?

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 URETERAL CATHETER CONNECTOR?

The FDA product code for URETERAL CATHETER CONNECTOR 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.

Other records listing Van-Tec, 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.

View all 52 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.

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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