3M CORNEAL SYSTEM (CORNEAL PRESERVATION MEDIUM)— 510(k) K863129

Name: FDA 510(k) clearance K863129
Creator: U.S. Food and Drug Administration
Published: 1986-09-17

Substantially Equivalent

3M Company

FDA 510(k) clearance K863129 for 3M CORNEAL SYSTEM (CORNEAL PRESERVATION MEDIUM), Substantially Equivalent on 1986-09-17. Applicant: 3M Company. Device class: Unclassified.

Clearance details

Applicant: 3M Company
Product code: Code LYX
Device class: Unclassified
Advisory panel: Unknown
Date received: 1986-08-15
Decision date: 1986-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

Download summary PDF View on FDA.gov ↗

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