K233307
- 510(k) number
- K233307
- Device name
- Intensity Pulsed Light Therapy System
- Applicant
- Beijing Adss Development Co., Ltd. CN
- Product code
- ONF — Powered Light Based Non-Laser Surgical Instrument Wi
- Decision date
- 2024-03-15
- Date received
- 2023-09-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K233307
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.