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)

PEDIATRIC ILLUMINATING URETERAL

K-Number: K832807 · 1983-10-19

ApplicantVan-Tec, Inc.
Decision Date1983-10-19
Product CodeFCW
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PEDIATRIC ILLUMINATING URETERAL 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 1983-10-19 under 510(k) number K832807. The device is classified under product code FCW. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEDIATRIC ILLUMINATING URETERAL?

PEDIATRIC ILLUMINATING URETERAL is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Van-Tec, Inc.. The 510(k) number is K832807.

When did PEDIATRIC ILLUMINATING URETERAL receive FDA 510(k) clearance?

PEDIATRIC ILLUMINATING URETERAL received FDA 510(k) clearance on 1983-10-19, under 510(k) number K832807.

Who is the listed applicant for PEDIATRIC ILLUMINATING URETERAL?

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 PEDIATRIC ILLUMINATING URETERAL?

The FDA product code for PEDIATRIC ILLUMINATING URETERAL is FCW.

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: FCW)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑