The following data is part of a premarket notification filed by Heartway Medical Products Co., Ltd. with the FDA for Heartway Power Chair, P23.
| Device ID | K100327 |
| 510k Number | K100327 |
| Device Name: | HEARTWAY POWER CHAIR, P23 |
| Classification | Wheelchair, Powered |
| Applicant | HEARTWAY MEDICAL PRODUCTS CO., LTD. ROC CHINESE- EUROPEAN IND. NO.58, FU-CHUIN STREET Hsin Chu City,,, Tw Hsq, TW 30067 |
| Contact | Ke-min Jen |
| Correspondent | Ke-min Jen HEARTWAY MEDICAL PRODUCTS CO., LTD. ROC CHINESE- EUROPEAN IND. NO.58, FU-CHUIN STREET Hsin Chu City,,, Tw Hsq, TW 30067 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-02-04 |
| Decision Date | 2010-03-22 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04719871230497 | K100327 | 000 |