Nephros
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2022-05-13
SEC Filings: 1 filings on record. Latest: 10-Q (2026-08-10). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K210575 | HDF Assist Mudule, HDF Infusion Set and Substitution Filter | KDI | 2022-05-13 | View |
No matching devices.