Nipro Medical Corporation
FDA 510(k) & PMA Approved Devices — 33 products
Advertisement
Total Devices33
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K261399 | ELISIO™-HX | QAX | 2026-07-28 | View |
| 510(k) | K253047 | PRESSONE™ | FMI | 2026-03-24 | View |
| 510(k) | K260533 | ELISIO™-H | KDI | 2026-03-19 | View |
| 510(k) | K222852 | Nipro SafeTouch Needle; Nipro Syringe with SafeTouch Needle | FMI | 2023-05-25 | View |
| 510(k) | K212677 | aboNT SYRINGE | FMF | 2022-04-15 | View |
| 510(k) | K190037 | Cronus HP PTA Balloon Catheter | LIT | 2019-10-24 | View |
| 510(k) | K191359 | Nipro Syringe | FMF | 2019-10-09 | View |
| 510(k) | K182940 | Surdial DX Hemodialysis System | KDI | 2019-07-19 | View |
| 510(k) | K173029 | Nipro Syringe | FMF | 2018-03-30 | View |
| 510(k) | K161681 | Nipro SafeTouch IV Catheter | FOZ | 2017-03-08 | View |
| 510(k) | K160444 | FB-U Hemodialyzer | KDI | 2017-02-08 | View |
| 510(k) | K151141 | Cronus HP - High Pressure Peripheral Balloon Catheter | LIT | 2016-01-14 | View |
| 510(k) | K131935 | ELISIO-H HEMODIALYZER, ELISIO-M HEMODIALYZER | KDI | 2013-12-20 | View |
| 510(k) | K131381 | ELISIO-H HEMODIALYZER | KDI | 2013-12-19 | View |
| 510(k) | K132153 | SAFETOUCH PSV WINGED INFUSION SET WITH/WITHOUT FILTER | FOZ | 2013-12-05 | View |
| 510(k) | K122952 | NIPRO PUREFLUX-L HEMODIALYZER | FJI | 2013-12-04 | View |
| 510(k) | K131641 | MONOJECT 60ML SYRINGE (LUER LOCK TIP, LUER SLIP TIP, CATHETER TIP) | FMF | 2013-08-28 | View |
| 510(k) | K122343 | PUREFLUX-H HEMODIALYZER | KDI | 2013-05-07 | View |
| 510(k) | K122347 | ELISIO-H AND ELISIO-M HEMODIALYZERS | KDI | 2013-05-01 | View |
| 510(k) | K130049 | MONOJECT 12ML SYRINGE | FMF | 2013-02-14 | View |
No matching devices.
Advertisement