MENICON NECT CONTACT LENS CASE— 510(k) K131875

Name: FDA 510(k) clearance K131875
Creator: U.S. Food and Drug Administration
Published: 2013-08-06

Substantially Equivalent

Foresight Regulatory Strategies

FDA 510(k) clearance K131875 for MENICON NECT CONTACT LENS CASE, Substantially Equivalent on 2013-08-06. Applicant: Foresight Regulatory Strategies. Device class: 2.

Clearance details

Applicant: Foresight Regulatory Strategies
Product code: Code LRX
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 2013-06-24
Decision date: 2013-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilmington, MA, US

Download summary PDF View on FDA.gov ↗

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