The following data is part of a premarket notification filed by Eye Think Eyewear with the FDA for Prestige Frames.
| Device ID | K940201 |
| 510k Number | K940201 |
| Device Name: | PRESTIGE FRAMES |
| Classification | Frame, Spectacle |
| Applicant | EYE THINK EYEWEAR 7535 KEELER AVE. Skokie, IL 60076 |
| Product Code | HQZ |
| CFR Regulation Number | 886.5842 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-01-13 |
| Decision Date | 1994-02-22 |