LED Phototherapy Device— 510(k) K162098
Substantially EquivalentLi-Tek Electronic Technology Corporation
FDA 510(k) clearance K162098 for LED Phototherapy Device, Substantially Equivalent on 2017-01-30. Applicant: Li-Tek Electronic Technology Corporation.
Clearance details
- Applicant
- Li-Tek Electronic Technology Corporation
- Product code
- Code OLP
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dongguan, CN
Adverse events under product code OLP
product code OLP- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.