The following data is part of a premarket notification filed by Wuxi Jiajian Medical Instrument Co., Ltd. with the FDA for Jiajian Tens.
Device ID | K112288 |
510k Number | K112288 |
Device Name: | JIAJIAN TENS |
Classification | Stimulator, Nerve, Transcutaneous, For Pain Relief |
Applicant | WUXI JIAJIAN MEDICAL INSTRUMENT CO., LTD. ROOM 1706, NO.128 SONGLE RD SONGJIANG AREA Shanghai, CN 201600 |
Contact | Doris Dong |
Correspondent | Doris Dong WUXI JIAJIAN MEDICAL INSTRUMENT CO., LTD. ROOM 1706, NO.128 SONGLE RD SONGJIANG AREA Shanghai, CN 201600 |
Product Code | GZJ |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-08-09 |
Decision Date | 2012-05-02 |
Summary: | summary |