EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS— 510(k) K941052

Name: FDA 510(k) clearance K941052
Creator: U.S. Food and Drug Administration
Published: 1994-04-12

Substantially Equivalent

Atlantic Optical Co., Inc.

FDA 510(k) clearance K941052 for EYEGLASS SPECTACLE FRAMES VARIOUS COLLECTIONS, Substantially Equivalent on 1994-04-12. Applicant: Atlantic Optical Co., Inc.. Device class: 1.

Clearance details

Applicant: Atlantic Optical Co., Inc.
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1994-03-03
Decision date: 1994-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chatsworth, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQZ

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K952597 — VIEW POINT, DORION, RUDDY PROJECT, ULTRA FLEX, TRILLON, BAY BOY, SHIELD SKI, SUN POCKETS, POINT OF VIEW1995-09-12
K944313 — SPECTACLE FRAME1995-03-28
K945176 — SPECTACLE FRAME OR EYEGLASS FRAMES1994-12-15
K945392 — SPECTACLE FRAME1994-12-15
K945770 — OPTICAL FRAMES1994-12-15

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K941555 — SUNGLASSES/VARIOUS COLLECTIONS1994-07-12
K912034 — VENETO COLLECTION1991-08-22

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