The following data is part of a premarket notification filed by Hoveround Corp. with the FDA for Hoveround Mpv.
| Device ID | K935410 |
| 510k Number | K935410 |
| Device Name: | HOVEROUND MPV |
| Classification | Wheelchair, Powered |
| Applicant | HOVEROUND CORP. 1748 INDEPENDENCE BLVD. SUITE B1 Sarasota, FL 34234 |
| Contact | Donald L Shapiro |
| Correspondent | Donald L Shapiro HOVEROUND CORP. 1748 INDEPENDENCE BLVD. SUITE B1 Sarasota, FL 34234 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent For Some Indications (SN) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-11-09 |
| Decision Date | 1994-03-28 |