The following data is part of a premarket notification filed by Golden Technologies, Inc. with the FDA for Golden Liteway.
| Device ID | K063162 |
| 510k Number | K063162 |
| Device Name: | GOLDEN LITEWAY |
| Classification | Vehicle, Motorized 3-wheeled |
| Applicant | GOLDEN TECHNOLOGIES, INC. 401 BRIDGE ST. Old Forge, PA 18518 |
| Contact | Gene R Kulon |
| Correspondent | Gene R Kulon GOLDEN TECHNOLOGIES, INC. 401 BRIDGE ST. Old Forge, PA 18518 |
| Product Code | INI |
| CFR Regulation Number | 890.3800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-10-18 |
| Decision Date | 2006-11-02 |
| Summary: | summary |