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 PMA

Excimer laser system

PMA Number: P030008 · 2025-01-16

ApplicantAlcon Laboratories, Inc.
Decision Date2025-01-16
PMA NumberP030008
Product CodeLZS
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOP

Device Summary

Excimer laser system is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories, Inc.. It received FDA 510(k) clearance on 2025-01-16. The device is classified under product code LZS. It was reviewed by the OP advisory panel.

Frequently Asked Questions

What is the Excimer laser system?

Excimer laser system is a medical device that received FDA 510(k) clearance on 2025-01-16. The listed applicant is Alcon Laboratories, Inc..

When did Excimer laser system receive FDA 510(k) clearance?

The clearance date for Excimer laser system can be found in the official FDA records.

Who is the listed applicant for Excimer laser system?

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

What is the FDA product code for Excimer laser system?

The FDA product code for Excimer laser system is LZS.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT04745156A Study Using Brain Stimulation and Behavioral Therapy to Increase Extent of Resection in Low-Grade GliomasNOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED

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.

↑