dermalux Flex MD— 510(k) K202028
Substantially EquivalentAesthetic Technology, Ltd.
FDA 510(k) clearance K202028 for dermalux Flex MD, Substantially Equivalent on 2020-12-16. Applicant: Aesthetic Technology, Ltd.. Device class: 2.
Clearance details
- Applicant
- Aesthetic Technology, Ltd.
- Product code
- Code ILY
- Device class
- Class 2
- Regulation
- 21 CFR 890.5500
- Advisory panel
- Physical Medicine
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Warrington, GB
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More clearances from Aesthetic Technology, Ltd.
view allAdverse events under product code ILY
product code ILY- Death
- 3
- Total
- 3
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.