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FDA 510(k)

OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED

K-Number: K921729 · 1992-06-09

ApplicantChiron Intraoptics
Decision Date1992-06-09
Product CodeLYX
DecisionSubstantially Equivalent

Device Summary

OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Chiron Intraoptics. It received FDA 510(k) clearance on 1992-06-09 under 510(k) number K921729. The device is classified under product code LYX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED?

OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED is a medical device that received FDA 510(k) clearance on 1992-06-09. The listed applicant is Chiron Intraoptics. The 510(k) number is K921729.

When did OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED receive FDA 510(k) clearance?

OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED received FDA 510(k) clearance on 1992-06-09, under 510(k) number K921729.

Who is the listed applicant for OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED?

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

What is the FDA product code for OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED?

The FDA product code for OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED 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 Chiron Intraoptics 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.

K925631PHACOTRON GOLD MULTIFUNCTION ULTRASONIC HANDPIECEK924165OPTISOL-GS CORNEAL STORAGE MEDIAK921728DEXSOL CORNEAL STORAGE MEDIA CONTAINER, MODIFIED

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.

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