Aomori Olympus Co., Ltd.
FDA 510(k) & PMA Approved Devices — 7 products
Advertisement
Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K042160 | SONOSURG TROCAR | LFL | 2005-01-25 | View |
| 510(k) | K041566 | SONOSURG ULTRASONIC SURGICAL SYSTEM | LFL | 2004-09-08 | View |
| 510(k) | K033333 | SINGLE USE 3-LUMEN BALLOON CATHETER, MODELS B-230Q-A AND B-230Q-B | FGE | 2003-11-14 | View |
| 510(k) | K031523 | OLYMPUS ULTRASONIC SURGICAL SYSTEM | LFL | 2003-10-01 | View |
| 510(k) | K031710 | OLYMPUS ULTRASONIC SURGICAL SYSTEM | LFL | 2003-08-29 | View |
| 510(k) | K021672 | PANCREATIC DRAINAGE TUBE | FGE | 2003-04-16 | View |
| 510(k) | K022446 | MUCUS COLLECTION PROBE, MODELS BC-401C & BC-402C | EOQ | 2003-03-28 | View |
No matching devices.
Advertisement