The following data is part of a premarket notification filed by Wuxi Jiajian Medical Instrument Co., Ltd. with the FDA for Jiajian Electro-acupuncture Stimulators.
Device ID | K122812 |
510k Number | K122812 |
Device Name: | JIAJIAN ELECTRO-ACUPUNCTURE STIMULATORS |
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 | 2012-09-13 |
Decision Date | 2013-04-11 |
Summary: | summary |