The following data is part of a premarket notification filed by Heartway Medical Products Co., Ltd. with the FDA for Heartway Lightweight Power Mobility Scooter, S34.
| Device ID | K101142 |
| 510k Number | K101142 |
| Device Name: | HEARTWAY LIGHTWEIGHT POWER MOBILITY SCOOTER, S34 |
| Classification | Vehicle, Motorized 3-wheeled |
| Applicant | HEARTWAY MEDICAL PRODUCTS CO., LTD. ROAD 25, NO. 6 TAICHUNG INDUSTRIAL PARK Taichung, TW 408 |
| Contact | Jen Ke-min |
| Correspondent | Jen Ke-min HEARTWAY MEDICAL PRODUCTS CO., LTD. ROAD 25, NO. 6 TAICHUNG INDUSTRIAL PARK Taichung, TW 408 |
| Product Code | INI |
| CFR Regulation Number | 890.3800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-04-22 |
| Decision Date | 2010-05-26 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04719871230435 | K101142 | 000 |