The following data is part of a premarket notification filed by Shenzhen Osto Technology Company Limited with the FDA for Health Expert Electronic Stimulator.
Device ID | K190673 |
510k Number | K190673 |
Device Name: | Health Expert Electronic Stimulator |
Classification | Stimulator, Nerve, Transcutaneous, Over-the-counter |
Applicant | Shenzhen OSTO Technology Company Limited No.43 Longfeng Road, Xinsheng Community, Longgang Street Longgang District, Shenzhen City, CN 518116 |
Contact | Li Yang |
Correspondent | Cassie Lee Guangzhou GLOMED Biological Technology Co., Ltd. Room 2231, Building 1, Ruifeng Center, Kaichuang Road Huangpu District Guangzhou, CN 51006 |
Product Code | NUH |
CFR Regulation Number | 882.5890 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-03-15 |
Decision Date | 2019-12-12 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
06950940801226 | K190673 | 000 |
06950940801370 | K190673 | 000 |
06950940801356 | K190673 | 000 |
06950940801561 | K190673 | 000 |
06950940801912 | K190673 | 000 |
06950940802155 | K190673 | 000 |
06950940802216 | K190673 | 000 |