Wat Medical Technology, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K230782 | TENS device-HeadaTerm 2 (Model: YF-HT2) | February 26, 2024 |
| K220503 | TENS device-EmeTerm 2, Model: YF-ZTY-E2 | April 23, 2022 |