Cold Sore Device (QPZ-03)— 510(k) K241155
Substantially EquivalentShenzhen Nuon Medical Equipment Co., Ltd.
FDA 510(k) clearance K241155 for Cold Sore Device (QPZ-03), Substantially Equivalent on 2024-09-05. Applicant: Shenzhen Nuon Medical Equipment Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Nuon Medical Equipment Co., Ltd.
- Product code
- Code OKJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.4860
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
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