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 |