The following data is part of a premarket notification filed by Senair-mot with the FDA for Kapper.
| Device ID | K904527 |
| 510k Number | K904527 |
| Device Name: | KAPPER |
| Classification | Syringe, Cartridge |
| Applicant | SENAIR-MOT 1118 E ADAMS AVE. Orange, CA 92667 |
| Contact | Richard G Deniro |
| Correspondent | Richard G Deniro SENAIR-MOT 1118 E ADAMS AVE. Orange, CA 92667 |
| Product Code | EJI |
| CFR Regulation Number | 872.6770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-10-02 |
| Decision Date | 1990-12-21 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() KAPPER 86816292 not registered Dead/Abandoned |
Keller Williams Realty, Inc. 2015-11-11 |
![]() KAPPER 86816275 not registered Dead/Abandoned |
Keller Williams Realty, Inc. 2015-11-11 |