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)

EUSOL-C

K-Number: K032422 · 2003-12-15

ApplicantAl.Chi.Mi.A
Decision Date2003-12-15
Product CodeLYX
DecisionSubstantially Equivalent

Device Summary

EUSOL-C is the device name listed in this FDA 510(k) record. The listed applicant is Al.Chi.Mi.A. It received FDA 510(k) clearance on 2003-12-15 under 510(k) number K032422. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EUSOL-C?

EUSOL-C is a medical device that received FDA 510(k) clearance on 2003-12-15. The listed applicant is Al.Chi.Mi.A. The 510(k) number is K032422.

When did EUSOL-C receive FDA 510(k) clearance?

EUSOL-C received FDA 510(k) clearance on 2003-12-15, under 510(k) number K032422.

Who is the listed applicant for EUSOL-C?

The FDA 510(k) record lists Al.Chi.Mi.A as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EUSOL-C?

The FDA product code for EUSOL-C is LYX.

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_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Al.Chi.Mi.A 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.

K063617EUSOL-C

Related Devices (Code: LYX)

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.

K251320XTRA4Al.Chi.Mi.A. S.R.LK221759CornisolAurolabK211786Independent Corneal Viewing Chamber (IVC-21)Bausch + Lomb, IncorporatedK162013Eusol-CAl.Chi.Mi.A. S.R.LK063304LIFE4CNumedis, Inc.K063617EUSOL-CAl.Chi.Mi.A

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.

↑