K242687
- 510(k) number
- K242687
- Device name
- NanoKnife Generator (H78720300301US0); NanoKnife Single Electrode Activation Probe, 15 cm (H787204001090); NanoKnife Single Electrode Activation Probe, 25 cm (H787204001100); NanoKnife Single Electrode Probe Spacer (H787204003010)
- Applicant
- AngioDynamics, Inc. MA · US
- Product code
- OAB — Low Energy Direct Current Thermal Ablation System
- Decision date
- 2024-12-06
- Date received
- 2024-09-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K242687.pdf
Official FDA record: K242687
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.