Ocg Technology, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K862947 | THE EXPERT MODELS RTS 2000 AND RTS 2000H | DSI | 1987-11-04 | View |
| 510(k) | K863153 | MODIFICATION OF CARDIOINTEGRAM/CARDIOINTEGRAPH | DXG | 1987-01-06 | View |
| 510(k) | K812971 | CARDIOINTEGRAM | DXG | 1981-12-29 | View |
No matching devices.
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