Wat Medical Technology (Ningbo) Co., Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K172450 | TENS device-HeadaTerm, eEspress | September 13, 2018 |
| K172478 | TENS device-EmeTerm, CinvStop | April 19, 2018 |