The following data is part of a premarket notification filed by Amigo Mobility Intl., Inc. with the FDA for Amigo Classic Fd.
| Device ID | K101507 |
| 510k Number | K101507 |
| Device Name: | AMIGO CLASSIC FD |
| Classification | Vehicle, Motorized 3-wheeled |
| Applicant | AMIGO MOBILITY INTL., INC. 6693 DIXIE HWY. Bridgeport, MI 48722 |
| Contact | Mike Labrake |
| Correspondent | Mike Labrake AMIGO MOBILITY INTL., INC. 6693 DIXIE HWY. Bridgeport, MI 48722 |
| Product Code | INI |
| CFR Regulation Number | 890.3800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-06-01 |
| Decision Date | 2010-07-30 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00863048000339 | K101507 | 000 |