The following data is part of a premarket notification filed by Vestil Manufacturing Corp. with the FDA for Jewel Mps.
| Device ID | K011374 |
| 510k Number | K011374 |
| Device Name: | JEWEL MPS |
| Classification | Wheelchair, Mechanical |
| Applicant | VESTIL MANUFACTURING CORP. P.O. BOX 507 Angola, IN 46703 |
| Contact | Rick Michael |
| Correspondent | Rick Michael VESTIL MANUFACTURING CORP. P.O. BOX 507 Angola, IN 46703 |
| Product Code | IOR |
| CFR Regulation Number | 890.3850 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-05-04 |
| Decision Date | 2001-05-29 |