The following data is part of a premarket notification filed by Amuchina Intl., Inc. with the FDA for Amuchina.
| Device ID | K952302 |
| 510k Number | K952302 |
| Device Name: | AMUCHINA |
| Classification | Disinfectant, Medical Devices |
| Applicant | AMUCHINA INTL., INC. 200 ORCHARD RIDGE DR. SUITE 220 Gaithersburg, MD 20878 |
| Product Code | LRJ |
| CFR Regulation Number | 880.6890 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-05-16 |
| Decision Date | 1995-07-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() AMUCHINA 76306402 2676881 Dead/Cancelled |
AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO A.C.R.A.F. S.P.A. 2001-08-29 |
![]() AMUCHINA 73540289 1382016 Dead/Cancelled |
AMUCHINA S.P.A. 1985-05-29 |