NEOLENS PRESCRIPTION SPECTACLE LENS— 510(k) K882814

Name: FDA 510(k) clearance K882814
Creator: U.S. Food and Drug Administration
Published: 1988-07-29

Substantially Equivalent

Neolens, Inc.

FDA 510(k) clearance K882814 for NEOLENS PRESCRIPTION SPECTACLE LENS, Substantially Equivalent on 1988-07-29. Applicant: Neolens, Inc.. Device class: 1.

Clearance details

Applicant: Neolens, Inc.
Product code: Code HQG
Device class: Class 1
Regulation: 21 CFR 886.5844
Advisory panel: Ophthalmic
Date received: 1988-07-08
Decision date: 1988-07-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

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