K252752
- 510(k) number
- K252752
- Device name
- ellacor System with Micro-Coring Technology
- Applicant
- Cytrellis Biosystems, Inc. MA · US
- Product code
- QAI — Powered Microneedle Device
- Decision date
- 2025-10-30
- Date received
- 2025-08-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K252752.pdf
Official FDA record: K252752
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.