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)

WILSON-COOK THRU-THE-SCOPE MECHANICAL LITHOTRIPTOR

K-Number: K011178 · 2001-05-04

Decision Date2001-05-04
Product CodeLQC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WILSON-COOK THRU-THE-SCOPE MECHANICAL LITHOTRIPTOR is the device name listed in this FDA 510(k) record. The listed applicant is Wilson-Cook Medical, Inc.. It received FDA 510(k) clearance on 2001-05-04 under 510(k) number K011178. The device is classified under product code LQC. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WILSON-COOK THRU-THE-SCOPE MECHANICAL LITHOTRIPTOR?

WILSON-COOK THRU-THE-SCOPE MECHANICAL LITHOTRIPTOR is a medical device that received FDA 510(k) clearance on 2001-05-04. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K011178.

When did WILSON-COOK THRU-THE-SCOPE MECHANICAL LITHOTRIPTOR receive FDA 510(k) clearance?

WILSON-COOK THRU-THE-SCOPE MECHANICAL LITHOTRIPTOR received FDA 510(k) clearance on 2001-05-04, under 510(k) number K011178.

Who is the listed applicant for WILSON-COOK THRU-THE-SCOPE MECHANICAL LITHOTRIPTOR?

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

What is the FDA product code for WILSON-COOK THRU-THE-SCOPE MECHANICAL LITHOTRIPTOR?

The FDA product code for WILSON-COOK THRU-THE-SCOPE MECHANICAL LITHOTRIPTOR is LQC.

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 Wilson-Cook Medical, 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 122 devices →

Related Devices (Code: LQC)

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.

↑