Integration Diagnostics, Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K033689 | OSSTELL MENTOR RFA | EKX | 2004-02-26 | View |
| 510(k) | K003714 | OSSTELL RESONANCE FREQUENCY ANALYZER | EKX | 2001-08-09 | View |
No matching devices.
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