The following data is part of a premarket notification filed by Vivid Optical Co., Ltd. with the FDA for Spectacle Frames.
| Device ID | K932992 |
| 510k Number | K932992 |
| Device Name: | SPECTACLE FRAMES |
| Classification | Frame, Spectacle |
| Applicant | VIVID OPTICAL CO., LTD. 2351 N.W. 93RD AVE. Miami, FL 33172 |
| Contact | Lorraine Cason |
| Correspondent | Lorraine Cason VIVID OPTICAL CO., LTD. 2351 N.W. 93RD AVE. Miami, FL 33172 |
| Product Code | HQZ |
| CFR Regulation Number | 886.5842 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-06-18 |
| Decision Date | 1993-10-01 |