SPECTACLE FRAME— 510(k) K932802

Name: FDA 510(k) clearance K932802
Creator: U.S. Food and Drug Administration
Published: 1993-09-09

Substantially Equivalent

Insight Optical Mfg. Co. of Florida, Inc.

FDA 510(k) clearance K932802 for SPECTACLE FRAME, Substantially Equivalent on 1993-09-09. Applicant: Insight Optical Mfg. Co. of Florida, Inc.. Device class: 1.

Clearance details

Applicant: Insight Optical Mfg. Co. of Florida, Inc.
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1993-06-09
Decision date: 1993-09-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hialeah, FL, US

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

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