WERAY— 510(k) K241963
Substantially EquivalentPicopack Co., Ltd.
FDA 510(k) clearance K241963 for WERAY, Substantially Equivalent on 2024-07-30. Applicant: Picopack Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Picopack Co., Ltd.
- Product code
- Code EHD
- Device class
- Class 2
- Regulation
- 21 CFR 872.1800
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Daejeon, KR
Recent devices under product code EHD
view allData sourced from openFDA. This site is unofficial and independent of the FDA.