The following data is part of a premarket notification filed by Freerider Usa, Inc. with the FDA for Freerider, Model Fr510-f.
| Device ID | K971387 |
| 510k Number | K971387 |
| Device Name: | FREERIDER, MODEL FR510-F |
| Classification | Vehicle, Motorized 3-wheeled |
| Applicant | FREERIDER USA, INC. 2322 DOUGLAS DR. Eugene, OR 97405 |
| Contact | Robert S Mcquate |
| Correspondent | Robert S Mcquate FREERIDER USA, INC. 2322 DOUGLAS DR. Eugene, OR 97405 |
| Product Code | INI |
| CFR Regulation Number | 890.3800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-04-14 |
| Decision Date | 1997-07-23 |
| Summary: | summary |