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 |