OPHTHALMIC SPECTACLE LENS BLANKS— 510(k) K881225

Name: FDA 510(k) clearance K881225
Creator: U.S. Food and Drug Administration
Published: 1988-04-19

Substantially Equivalent

Beta Optical Co, Inc.

FDA 510(k) clearance K881225 for OPHTHALMIC SPECTACLE LENS BLANKS, Substantially Equivalent on 1988-04-19. Applicant: Beta Optical Co, Inc.. Device class: 1.

Clearance details

Applicant: Beta Optical Co, Inc.
Product code: Code HQG
Device class: Class 1
Regulation: 21 CFR 886.5844
Advisory panel: Ophthalmic
Date received: 1988-03-22
Decision date: 1988-04-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Davie, FL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HQG

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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

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