SPECTACLE FRAMES— 510(k) K930435
Substantially EquivalentVenis 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
Recent devices under product code HOI
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