The following data is part of a premarket notification filed by Sunpex Technology Co., Ltd. with the FDA for Sunpex Technologies Model Pw.
| Device ID | K024175 |
| 510k Number | K024175 |
| Device Name: | SUNPEX TECHNOLOGIES MODEL PW |
| Classification | Wheelchair, Powered |
| Applicant | SUNPEX TECHNOLOGY CO., LTD. 914 WEST PATAPSCO AVE. Baltimore, MD 21230 |
| Contact | Leonard Frier |
| Correspondent | Leonard Frier SUNPEX TECHNOLOGY CO., LTD. 914 WEST PATAPSCO AVE. Baltimore, MD 21230 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-12-18 |
| Decision Date | 2003-05-01 |