K231738
- 510(k) number
- K231738
- Device name
- NEUWAVE Microwave Ablation System and Accessories
- Applicant
- Neuwave Medical, Inc. WI · US
- Product code
- NEY — System, Ablation, Microwave And Accessories
- Decision date
- 2023-11-16
- Date received
- 2023-06-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K231738.pdf
Official FDA record: K231738
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.