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 |