510(k) K220385
K220385 is an FDA 510(k) premarket notification submitted by Beijing Globalipl Development Co., Ltd. for the device "Intense Pulsed Light Equipment". The FDA issued a decision of Substantially Equivalent on August 12, 2022. The device falls under product code ONF (Powered Light Based Non-Laser Surgical Instrument With Thermal Effect), a Class II device regulated under 21 CFR 878.4810. Beijing Globalipl Development Co., Ltd. has at least 3 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 12, 2022
- Date Received
- February 10, 2022
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
- Device Class
- Class II
- Regulation Number
- 878.4810
- Review Panel
- SU
- Submission Type
A light based non-laser device that provides thermal effect including broad spectrum source devices such as intense pulse light (ipl). Typically, indicated to be used in medical specialties of general and plastic surgery and of dermatology/aesthetic. Indication for use can be general and/or specific.The classification regulation 21 cfr 878.4810 describes a device that is carbon dioxide or argon laser intended to cut, destroy, or remove tissue by the light.