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)

BILIARY STONE DISLODGER

K-Number: K925559 · 1992-12-17

Decision Date1992-12-17
Product CodeLQR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

BILIARY STONE DISLODGER is the device name listed in this FDA 510(k) record. The listed applicant is Annex Medical, Inc.. It received FDA 510(k) clearance on 1992-12-17 under 510(k) number K925559. The device is classified under product code LQR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BILIARY STONE DISLODGER?

BILIARY STONE DISLODGER is a medical device that received FDA 510(k) clearance on 1992-12-17. The listed applicant is Annex Medical, Inc.. The 510(k) number is K925559.

When did BILIARY STONE DISLODGER receive FDA 510(k) clearance?

BILIARY STONE DISLODGER received FDA 510(k) clearance on 1992-12-17, under 510(k) number K925559.

Who is the listed applicant for BILIARY STONE DISLODGER?

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

What is the FDA product code for BILIARY STONE DISLODGER?

The FDA product code for BILIARY STONE DISLODGER is LQR.

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 Annex 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 23 devices →

Related Devices (Code: LQR)

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.

↑