SPECTACLE PRESCRIPTION LENSES— 510(k) K853110

Name: FDA 510(k) clearance K853110
Creator: U.S. Food and Drug Administration
Published: 1985-08-09

Substantially Equivalent

Ancie Laboratories

FDA 510(k) clearance K853110 for SPECTACLE PRESCRIPTION LENSES, Substantially Equivalent on 1985-08-09. Applicant: Ancie Laboratories. Device class: 1.

Clearance details

Applicant: Ancie Laboratories
Product code: Code HQG
Device class: Class 1
Regulation: 21 CFR 886.5844
Advisory panel: Ophthalmic
Date received: 1985-07-24
Decision date: 1985-08-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lanham, MD, US

Download summary PDF View on FDA.gov ↗

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K884360 — SEIKO P-6 PROGRESSIVE SPECTACLE LENSES1988-11-15
K882814 — NEOLENS PRESCRIPTION SPECTACLE LENS1988-07-29

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