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 |