The following data is part of a premarket notification filed by Wuxi Jiajian Medical Instrument Co., Ltd. with the FDA for Jiajian Cmn Stimulator.
| Device ID | K130768 |
| 510k Number | K130768 |
| Device Name: | JIAJIAN CMN STIMULATOR |
| Classification | Stimulator, Electro-acupuncture |
| 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 | BWK |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-03-20 |
| Decision Date | 2013-08-16 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00810011252509 | K130768 | 000 |
| 10815005022400 | K130768 | 000 |
| 08150050225006 | K130768 | 000 |