The following data is part of a premarket notification filed by Medico Usa Inc. with the FDA for Miin.
| Device ID | K193266 |
| 510k Number | K193266 |
| Device Name: | MIIN |
| Classification | Powered Laser Surgical Instrument |
| Applicant | Medico USA Inc. 3407 W 6th St Suite 507 Los Angeles, CA 90020 |
| Contact | Peter Son |
| Correspondent | Joyce Kwon Provision Consulting Group Inc. 100 Barranca St. Suite 700 West Covina, CA 91791 |
| Product Code | GEX |
| CFR Regulation Number | 878.4810 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-11-26 |
| Decision Date | 2021-01-22 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MIIN 85944801 4462624 Live/Registered |
R.J Max, Inc. 2013-05-29 |