K233709
- 510(k) number
- K233709
- Device name
- Exceed Unlimited
- Applicant
- Mt. Derm GmbH DE
- Product code
- QAI — Powered Microneedle Device
- Decision date
- 2024-02-23
- Date received
- 2023-11-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K233709.pdf
Official FDA record: K233709
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.