The following data is part of a premarket notification filed by Venis Di Alessandro Vendrame with the FDA for Spectacle Frames.
| Device ID | K930597 |
| 510k Number | K930597 |
| Device Name: | SPECTACLE FRAMES |
| Classification | Frame, Spectacle |
| Applicant | VENIS DI ALESSANDRO VENDRAME VIA LEONARDO DA VINCI, 4 31013 CODOGNE Treviso, Italy, IT |
| Contact | Vendrame Alessandro |
| Correspondent | Vendrame Alessandro VENIS DI ALESSANDRO VENDRAME VIA LEONARDO DA VINCI, 4 31013 CODOGNE Treviso, Italy, IT |
| Product Code | HQZ |
| CFR Regulation Number | 886.5842 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-02-05 |
| Decision Date | 1993-08-02 |