The following data is part of a premarket notification filed by Jintronix Inc. with the FDA for Jintronix.
| Device ID | K143034 |
| 510k Number | K143034 |
| Device Name: | Jintronix |
| Classification | Interactive Rehabilitation Exercise Devices |
| Applicant | JINTRONIX INC. 999 3rd Ave, Suite 3400 Seattle, WA 98104 |
| Contact | Mark Evin |
| Correspondent | Navneet Sekhon AxSource Consulting Inc. 336 Bronte Street Suite 224-225 Milton, CA L9t 7w6 |
| Product Code | LXJ |
| CFR Regulation Number | 890.5360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-10-22 |
| Decision Date | 2015-04-22 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() JINTRONIX 88331342 5894982 Live/Registered |
Jintronix, Inc. 2019-03-08 |
![]() JINTRONIX 88331336 5894981 Live/Registered |
Jintronix, Inc. 2019-03-08 |