SPECTACLE FRAME— 510(k) K944313

Name: FDA 510(k) clearance K944313
Creator: U.S. Food and Drug Administration
Published: 1995-03-28

Substantially Equivalent

Sun Hing Optical Manufactory , Ltd.

FDA 510(k) clearance K944313 for SPECTACLE FRAME, Substantially Equivalent on 1995-03-28. Applicant: Sun Hing Optical Manufactory , Ltd.. Device class: 1.

Clearance details

Applicant: Sun Hing Optical Manufactory , Ltd.
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1994-08-29
Decision date: 1995-03-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kwun Tong, Kowloon, Hong Kong, HK

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
K945176 — SPECTACLE FRAME OR EYEGLASS FRAMES1994-12-15
K945392 — SPECTACLE FRAME1994-12-15
K945770 — OPTICAL FRAMES1994-12-15
K945350 — FRAME, SPECTACLES1994-12-13

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