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)

ENDO-TRIPTON, MECHANICAL GALLSTONE CRUSHER

K-Number: K860863 · 1986-05-15

Decision Date1986-05-15
Product CodeLQC
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDO-TRIPTON, MECHANICAL GALLSTONE CRUSHER is the device name listed in this FDA 510(k) record. The listed applicant is George Percy Mcgown. It received FDA 510(k) clearance on 1986-05-15 under 510(k) number K860863. 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 ENDO-TRIPTON, MECHANICAL GALLSTONE CRUSHER?

ENDO-TRIPTON, MECHANICAL GALLSTONE CRUSHER is a medical device that received FDA 510(k) clearance on 1986-05-15. The listed applicant is George Percy Mcgown. The 510(k) number is K860863.

When did ENDO-TRIPTON, MECHANICAL GALLSTONE CRUSHER receive FDA 510(k) clearance?

ENDO-TRIPTON, MECHANICAL GALLSTONE CRUSHER received FDA 510(k) clearance on 1986-05-15, under 510(k) number K860863.

Who is the listed applicant for ENDO-TRIPTON, MECHANICAL GALLSTONE CRUSHER?

The FDA 510(k) record lists George Percy Mcgown as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDO-TRIPTON, MECHANICAL GALLSTONE CRUSHER?

The FDA product code for ENDO-TRIPTON, MECHANICAL GALLSTONE CRUSHER 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.

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.

↑