OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED— 510(k) K921729

Name: FDA 510(k) clearance K921729
Creator: U.S. Food and Drug Administration
Published: 1992-06-09

Substantially Equivalent

Chiron Intraoptics

FDA 510(k) clearance K921729 for OPTISOL CORNEAL STORAGE MEDIA CONTAINER/MODIFIED, Substantially Equivalent on 1992-06-09. Applicant: Chiron Intraoptics. Device class: Unclassified.

Clearance details

Applicant: Chiron Intraoptics
Product code: Code LYX
Device class: Unclassified
Advisory panel: Unknown
Date received: 1992-03-25
Decision date: 1992-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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