FDA 510(k)
FDA class 2
Substantially Equivalent
🇨🇳 China
Intense Pulsed Light Therapy Device
K Number: K261204
·
Decision Jun 12, 2026
Classifications
1
FEI Numbers
92
Registration Numbers
93
Same Product Code
73
Applicant Total
1
Review Days
60
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Basic Information
- Device Name
- Intense Pulsed Light Therapy Device
- K Number
- K261204
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4810
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Sanhe LEFIS Electronics Co., Ltd.
- Date Received
- April 13, 2026
- Decision Date
- June 12, 2026
- Product Code
- ONF
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| ONF | Powered Light Based Non-Laser Surgical Instrument With Thermal Effect | FDA class 2 | General, Plastic Surgery |
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