Cardio Design Pty. , 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) | K983052 | PERITRON PERINEOMETER MODEL 9300V OR 9300A | HIR | 1998-10-19 | View |
| 510(k) | K945611 | PERITRON | HIR | 1996-02-08 | View |
No matching devices.
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