The following data is part of a premarket notification filed by Everest & Jennings, Inc. with the FDA for Ultra-lite Premier.
| Device ID | K841830 |
| 510k Number | K841830 |
| Device Name: | ULTRA-LITE PREMIER |
| Classification | Wheelchair, Mechanical |
| Applicant | EVEREST & JENNINGS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IOR |
| CFR Regulation Number | 890.3850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1984-05-03 |
| Decision Date | 1984-05-14 |