TENS device-HeadaTerm 2 (Model: YF-HT2)— 510(k) K230782
Substantially EquivalentWat Medical Technology, Inc.
FDA 510(k) clearance K230782 for TENS device-HeadaTerm 2 (Model: YF-HT2), Substantially Equivalent on 2024-02-26. Applicant: Wat Medical Technology, Inc..
Clearance details
- Applicant
- Wat Medical Technology, Inc.
- Product code
- Code PCC
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ningbo, CN
Adverse events under product code PCC
product code PCC- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.