Renovorx, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2021-08-23
SEC Filings: 1 filings on record. Latest: 8-K (2026-08-04). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K212324 | RenovoCath | MJN | 2021-08-23 | View |
| 510(k) | K191606 | RenovoCath | MJN | 2019-08-07 | View |
| 510(k) | K160067 | RenovoCath | MJN | 2017-03-07 | View |
No matching devices.