Prothia USA, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
Advertisement
Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K831071 | UNIVERSAL INSTRU. SET FOR NEUROVASCULAR | GZX | 1983-06-08 | View |
| 510(k) | K830993 | AMPLIGREFFE | GFD | 1983-05-03 | View |
| 510(k) | K823581 | ELPHA 500 | GCJ | 1983-03-24 | View |
| 510(k) | K830058 | MYOGRAPH 2000 | BXN | 1983-03-07 | View |
| 510(k) | K823583 | MYOTEST NERVE STIMULATOR | BXN | 1982-12-30 | View |
No matching devices.
Advertisement