Clearance Summary
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) received FDA 510(k) clearance under submission number K242687, sponsored by AngioDynamics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2024-12-06.
- Submission: K242687
- Applicant / Sponsor: AngioDynamics, Inc.
- Clearance pathway: Traditional
- Review panel: General, Plastic Surgery
- Device class: Class II
- Regulation citation: 21 CFR 878.4400
- Decision date: 2024-12-06
Classification & Regulation
This clearance is catalogued under FDA product code OAB and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.