The following data is part of a premarket notification filed by Mi Mun Corp. with the FDA for Spectacle Frames Or Eyeglass Frames.
| Device ID | K945340 |
| 510k Number | K945340 |
| Device Name: | SPECTACLE FRAMES OR EYEGLASS FRAMES |
| Classification | Frame, Spectacle |
| Applicant | MI MUN CORP. 1076-1, PYUNGRI-DONG, SEO-GU Daegu, KR 703013 |
| Contact | Hwi-sung Lim |
| Correspondent | Hwi-sung Lim MI MUN CORP. 1076-1, PYUNGRI-DONG, SEO-GU Daegu, KR 703013 |
| Product Code | HQZ |
| CFR Regulation Number | 886.5842 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-11-01 |
| Decision Date | 1994-11-22 |