LEM SPECTACLE FRAMES DIFFERENT COLORS AND DESIGNS— 510(k) K870220

Name: FDA 510(k) clearance K870220
Creator: U.S. Food and Drug Administration
Published: 1987-04-16

Substantially Equivalent

Lem Srl.

FDA 510(k) clearance K870220 for LEM SPECTACLE FRAMES DIFFERENT COLORS AND DESIGNS, Substantially Equivalent on 1987-04-16. Applicant: Lem Srl.. Device class: 1.

Clearance details

Applicant: Lem Srl.
Product code: Code HQZ
Device class: Class 1
Regulation: 21 CFR 886.5842
Advisory panel: Ophthalmic
Date received: 1987-01-21
Decision date: 1987-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Italy, IT

Download summary PDF View on FDA.gov ↗

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K945392 — SPECTACLE FRAME1994-12-15
K945770 — OPTICAL FRAMES1994-12-15

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K870219 — LEM SUNGLASSES & FRAMES DIFF. COLORS AND DESIGNS1987-04-16

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