Roger Cestac & Assoc.
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) | K811750 | MULTITUBULAR THORACIC AIR SPLINTS | IPT | 1981-07-20 | View |
| 510(k) | K811704 | MULTITUBULAR AIR SPLINT KIT | IQI | 1981-07-01 | View |
No matching devices.
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