Angiodynamics
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2026-03-24
SEC Filings: 1 filings on record. Latest: 10-K (2026-07-14). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253198 | NanoKnife Generator (H78720300351US0) | OAB | 2026-03-24 | View |
| 510(k) | K183385 | NanoKnife System | OAB | 2019-06-18 | View |
No matching devices.
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