The following data is part of a premarket notification filed by Vestil Manufacturing Corp. with the FDA for Magic Mobility 4 X 4 Wheelchair.
| Device ID | K000796 |
| 510k Number | K000796 |
| Device Name: | MAGIC MOBILITY 4 X 4 WHEELCHAIR |
| Classification | Wheelchair, Powered |
| Applicant | VESTIL MANUFACTURING CORP. 900 GROWTH PKWY. Angola, IN 46703 |
| Contact | Rick Michael |
| Correspondent | Rick Michael VESTIL MANUFACTURING CORP. 900 GROWTH PKWY. Angola, IN 46703 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-03-13 |
| Decision Date | 2000-08-11 |