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 |