Sunscope Intl., Inc.
FDA 510(k) & PMA Approved Devices — 7 products
Advertisement
Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K002786 | BIOSENSORS CENTRAL VENOUS CATHETER KITS | FOZ | 2000-11-17 | View |
| 510(k) | K983372 | BIOPORT CLOSED BLOOD SAMPLING SYSTEM, MODEL BT XXXXXX- BP | DRS | 1999-02-05 | View |
| 510(k) | K973477 | BIOSENSORS EMBOLECTOMY CATHETER | DXE | 1998-09-04 | View |
| 510(k) | K981747 | BIOTRANS PRESSURE MONITORING KIT MODEL NUMBER BT XXXXXX | DRS | 1998-08-20 | View |
| 510(k) | K981745 | BIOTRANS REUSABLE SENSOR BASE MODEL NUMBER BT XXXXXX | DRS | 1998-07-17 | View |
| 510(k) | K911710 | HEPARIN COATED THERMODILUTION CATH & ACCESSORIES | DQO | 1991-10-23 | View |
| 510(k) | K912172 | SAFEWEDGE(TM) RELIEF VALVE DEVICE | KRB | 1991-09-27 | View |
No matching devices.
Advertisement