Simbionix , Ltd.
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) | K123269 | PROCEDURE REHEARSAL STUDIO | LLZ | 2013-01-29 | View |
| 510(k) | K112387 | PROCEDURE REHEARSAL STUDIO(TM) | LLZ | 2011-12-27 | View |
| 510(k) | K093269 | PROCEDURE REHEARSAL STUDIO | LLZ | 2010-08-20 | View |
No matching devices.
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