510(k) K242687 ยท OAB Low Energy Direct Current Thermal Ablation System
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., Marlborough MA, US |
| Decision | Substantially Equivalent, Dec 6, 2024 |
| Received | Sep 6, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242687
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.