The following data is part of a premarket notification filed by Heartway Medical Products Co., Ltd. with the FDA for Heartway Power Mobility Scooter, S11.
Device ID | K101143 |
510k Number | K101143 |
Device Name: | HEARTWAY POWER MOBILITY SCOOTER, S11 |
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 |
---|---|---|
04719871230145 | K101143 | 000 |