APEX OPTICAL IND. CO., EYE WEA MODELS— 510(k) K932821

Name: FDA 510(k) clearance K932821
Creator: U.S. Food and Drug Administration
Published: 1994-01-25

Substantially Equivalent

Apex Optical Ind. Co.

FDA 510(k) clearance K932821 for APEX OPTICAL IND. CO., EYE WEA MODELS, Substantially Equivalent on 1994-01-25. Applicant: Apex Optical Ind. Co.. Device class: 1.

Clearance details

Applicant: Apex Optical Ind. Co.
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1993-06-09
Decision date: 1994-01-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Daegu, Korea, KR

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQZ

view all

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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