The following data is part of a premarket notification filed by Jerry Medical Instrument (shanghai) Co., Ltd. with the FDA for Electric Wheelchair [models: Jrwd6010/jrwd6012].
Device ID | K192739 |
510k Number | K192739 |
Device Name: | Electric Wheelchair [Models: JRWD6010/JRWD6012] |
Classification | Wheelchair, Powered |
Applicant | Jerry Medical Instrument (Shanghai) Co., Ltd. Building 12, No. 615 Fengdeng Rd, Malu Town, Jiading District Shanghai, CN 201801 |
Contact | Jianguo Chen |
Correspondent | Boyle Wang Shanghai Truthful Information Technology Co., Ltd. RM.608, No.738, Shangcheng Rd., Pudong Shanghai, CN 200120 |
Product Code | ITI |
CFR Regulation Number | 890.3860 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-09-30 |
Decision Date | 2021-07-13 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06934374100278 | K192739 | 000 |
06934374100261 | K192739 | 000 |