J.A. Preston Corp.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K861739 | TEC PORTAMAX H.V. PULSED GALVANIC STIMULATOR | IPF | 1986-06-09 | View |
| 510(k) | K830747 | PC 2909A-HEALTH PULSE CONTROL STIMULATOR | GZJ | 1983-05-30 | View |
No matching devices.
Advertisement