The following data is part of a premarket notification filed by Matrix Medica, Inc. with the FDA for Klorman.
Device ID | K923693 |
510k Number | K923693 |
Device Name: | KLORMAN |
Classification | Disinfectant, Medical Devices |
Applicant | MATRIX MEDICA, INC. 145 MID COUNTY DR. Orchard Park, NY |
Contact | Michael Swart |
Correspondent | Michael Swart MATRIX MEDICA, INC. 145 MID COUNTY DR. Orchard Park, NY |
Product Code | LRJ |
CFR Regulation Number | 880.6890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-07-23 |
Decision Date | 1996-01-23 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
KLORMAN 73723570 1532893 Live/Registered |
CONTROL CHEMICALS (PROPRIETARY) LIMITED 1988-04-20 |