K251111
- 510(k) number
- K251111
- Device name
- Cary
- Applicant
- Excitus AS NO
- Product code
- JCX — Apparatus, Suction, Ward Use, Portable, Ac-Powered
- Decision date
- 2025-05-07
- Date received
- 2025-04-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Flag
- Third-party review
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K251111.pdf
Official FDA record: K251111
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.