EYEDENTITY EYEWEAR— 510(k) K872062

Name: FDA 510(k) clearance K872062
Creator: U.S. Food and Drug Administration
Published: 1987-06-12

Substantially Equivalent

Vitech Research C/O Johnsen, Manfredi & Thorpe

FDA 510(k) clearance K872062 for EYEDENTITY EYEWEAR, Substantially Equivalent on 1987-06-12. Applicant: Vitech Research C/O Johnsen, Manfredi & Thorpe. Device class: 1.

Clearance details

Applicant: Vitech Research C/O Johnsen, Manfredi & Thorpe
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1987-05-28
Decision date: 1987-06-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Los Angeles, CA, 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

More clearances from Vitech Research C/O Johnsen, Manfredi & Thorpe

view all

K851039 — EYEDENTITY EYEWEAR1985-04-01

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