The following data is part of a premarket notification filed by Everest & Jennings, Inc. with the FDA for Universal Wheelchair.
| Device ID | K930411 |
| 510k Number | K930411 |
| Device Name: | UNIVERSAL WHEELCHAIR |
| Classification | Wheelchair, Mechanical |
| Applicant | EVEREST & JENNINGS, INC. 3601 RIDER TRAIL SOUTH Earth City, MO 63045 |
| Contact | Jackie Wilkins |
| Correspondent | Jackie Wilkins EVEREST & JENNINGS, INC. 3601 RIDER TRAIL SOUTH Earth City, MO 63045 |
| Product Code | IOR |
| CFR Regulation Number | 890.3850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-01-26 |
| Decision Date | 1993-03-31 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00822383582788 | K930411 | 000 |
| 00822383145280 | K930411 | 000 |
| 00822383140483 | K930411 | 000 |
| 00822383133904 | K930411 | 000 |
| 00822383133867 | K930411 | 000 |
| 00822383133850 | K930411 | 000 |
| 00822383123356 | K930411 | 000 |
| 50822383269837 | K930411 | 000 |
| 50885380046368 | K930411 | 000 |
| 50885380046344 | K930411 | 000 |
| 50885380046320 | K930411 | 000 |
| 00822383269788 | K930411 | 000 |
| 00822383269795 | K930411 | 000 |
| 50822383567803 | K930411 | 000 |
| 00822383567808 | K930411 | 000 |
| 00822383526539 | K930411 | 000 |
| 00822383289670 | K930411 | 000 |
| 00822383289663 | K930411 | 000 |
| 00822383289656 | K930411 | 000 |
| 00822383289632 | K930411 | 000 |
| 00822383289618 | K930411 | 000 |
| 00822383269849 | K930411 | 000 |
| 00822383269801 | K930411 | 000 |
| 00822383289649 | K930411 | 000 |