SPECTACLE FRAMES— 510(k) K930435

Substantially Equivalent

Venis DI A. Vendrame

FDA 510(k) clearance K930435 for SPECTACLE FRAMES, Substantially Equivalent on 1993-09-20. Applicant: Venis DI A. Vendrame. Device class: 1.

Clearance details

Applicant
Venis DI A. Vendrame
Product code
Code HOI
Device class
Class 1
Regulation
21 CFR 886.5840
Advisory panel
Ophthalmic
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Treviso, Italy, IT
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