MULTIPLE SPECTACLE LENS— 510(k) K871961

Name: FDA 510(k) clearance K871961
Creator: U.S. Food and Drug Administration
Published: 1987-06-03

Substantially Equivalent

Korea Asahi Optical Co., Ltd.

FDA 510(k) clearance K871961 for MULTIPLE SPECTACLE LENS, Substantially Equivalent on 1987-06-03. Applicant: Korea Asahi Optical Co., Ltd.. Device class: 1.

Clearance details

Applicant: Korea Asahi Optical Co., Ltd.
Product code: Code HQG
Device class: Class 1
Regulation: 21 CFR 886.5844
Advisory panel: Ophthalmic
Date received: 1987-05-20
Decision date: 1987-06-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Seoul, Korea, KR

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQG

view all

K935919 — SUNGLASSES1994-02-16
K920795 — 0R 160, OR-1.60, AND ORCOLITE 1.60 HIGH INDEX1992-07-13
K900091 — MODIFIED OPHTHALMIC OPIR ONUFRYK IMAGE DEFLECTOR1990-04-04
K884360 — SEIKO P-6 PROGRESSIVE SPECTACLE LENSES1988-11-15
K882814 — NEOLENS PRESCRIPTION SPECTACLE LENS1988-07-29

More clearances from Korea Asahi Optical Co., Ltd.

view all

K871649 — CLASSIC 70 LENS1987-05-29

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