The following data is part of a premarket notification filed by Tisport, Llc with the FDA for Tilite Evo.
| Device ID | K024055 |
| 510k Number | K024055 |
| Device Name: | TILITE EVO |
| Classification | Wheelchair, Mechanical |
| Applicant | TISPORT, LLC 1426 EAST THIRD AVE. Kennewick, WA 99337 -9669 |
| Contact | Richard S Foreman |
| Correspondent | Richard S Foreman TISPORT, LLC 1426 EAST THIRD AVE. Kennewick, WA 99337 -9669 |
| Product Code | IOR |
| CFR Regulation Number | 890.3850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-12-09 |
| Decision Date | 2002-12-20 |
| Summary: | summary |