POLARIS CONTACT LENS CASE— 510(k) K093377

Name: FDA 510(k) clearance K093377
Creator: U.S. Food and Drug Administration
Published: 2010-04-27

Substantially Equivalent

Reliance Design & Manufacturing Corp.

FDA 510(k) clearance K093377 for POLARIS CONTACT LENS CASE, Substantially Equivalent on 2010-04-27. Applicant: Reliance Design & Manufacturing Corp.. Device class: 2.

Clearance details

Applicant: Reliance Design & Manufacturing Corp.
Product code: Code LRX
Device class: Class 2
Regulation: 21 CFR 886.5928
Advisory panel: Ophthalmic
Date received: 2009-10-29
Decision date: 2010-04-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Keelung, TW

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.