The following data is part of a premarket notification filed by Peak Performance Technologies, Inc with the FDA for Peak Motus.
| Device ID | K030714 |
| 510k Number | K030714 |
| Device Name: | PEAK MOTUS |
| Classification | Interactive Rehabilitation Exercise Devices |
| Applicant | PEAK PERFORMANCE TECHNOLOGIES, INC 7388 S. REVERE PKY 901 Centinnial, CO 80112 |
| Contact | Larry Scheirman |
| Correspondent | Larry Scheirman PEAK PERFORMANCE TECHNOLOGIES, INC 7388 S. REVERE PKY 901 Centinnial, CO 80112 |
| Product Code | LXJ |
| CFR Regulation Number | 890.5360 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-03-06 |
| Decision Date | 2003-05-16 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PEAK MOTUS 75065330 2094353 Dead/Cancelled |
Peak Performance Technologies, Inc. 1996-02-29 |