The following data is part of a premarket notification filed by Freerider Corp with the FDA for Freerider Fr1, Models Fr1-13, Fr1-15, Fr1-17.
| Device ID | K133187 |
| 510k Number | K133187 |
| Device Name: | FREERIDER FR1, Models FR1-13, FR1-15, FR1-17 |
| Classification | Vehicle, Motorized 3-wheeled |
| Applicant | FREERIDER CORP 8696 UTICA AVE Rancho Cucamonga, CA 91730 |
| Contact | Aaron Chang |
| Correspondent | Aaron Chang FREERIDER CORP 8696 UTICA AVE Rancho Cucamonga, CA 91730 |
| Product Code | INI |
| CFR Regulation Number | 890.3800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-10-17 |
| Decision Date | 2015-01-08 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04713072966032 | K133187 | 000 |
| 04713072966049 | K133187 | 000 |
| 04713072962393 | K133187 | 000 |