Northeast Scientific, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories3
Latest FDA decision2025-05-12
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K250592 | NES Reprocessed Visions PV .018 Digital IVUS Catheter (R-86700) | OWQ | 2025-05-12 | View |
| 510(k) | K223026 | NES Reprocessed Eagle Eye Platinum RX Digital IVUS Catheter | OWQ | 2023-02-03 | View |
| 510(k) | K220171 | NES Reprocessed 0.9mm Turbo Elite Laser Atherectomy Catheter | QTF | 2022-07-01 | View |
| 510(k) | K200195 | NES Reprocessed Visions PV .014P RX Digital IVUS Catheter | OBJ | 2020-06-22 | View |
No matching devices.