Intense Pulse Light Therapeutic Apparatus— 510(k) K232932
Substantially EquivalentShenzhen Greatro Electronic Technology Co., Ltd.
FDA 510(k) clearance K232932 for Intense Pulse Light Therapeutic Apparatus, Substantially Equivalent on 2023-12-04. Applicant: Shenzhen Greatro Electronic Technology Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Greatro Electronic Technology Co., Ltd.
- Product code
- Code OHT
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
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More clearances from Shenzhen Greatro Electronic Technology Co., Ltd.
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