BRILLETTE MODEL— 510(k) K842835

Substantially Equivalent

Cillus Company, Inc.

FDA 510(k) clearance K842835 for BRILLETTE MODEL, Substantially Equivalent on 1984-11-21. Applicant: Cillus Company, Inc.. Device class: 1.

Clearance details

Applicant: Cillus Company, Inc.
Product code: Code HOI
Device class: Class 1
Regulation: 21 CFR 886.5840
Advisory panel: Ophthalmic
Date received: 1984-07-20
Decision date: 1984-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Novato, CA, US

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K931328 — PYRAMID SUNGLASSES/PYRAMID READING GLASSES1993-08-10
K910329 — SUNGLASSES1991-03-12
K854854 — SYSTEMS OF SIGHT LOW VISION EYEWARE1986-02-04

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