Superdimension, Ltd.
FDA 510(k) & PMA Approved Devices — 10 products
Advertisement
Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K102604 | I-LOGIC INREACH SYSTEM | JAK | 2010-10-07 | View |
| 510(k) | K092365 | INREACH SYSTEM, MODEL AAS00161-02 | JAK | 2009-09-04 | View |
| 510(k) | K082386 | INREACH PLANNING LAPTOP | LLZ | 2008-09-16 | View |
| 510(k) | K081379 | MODIFICATION TO INREACH SYSTEM | JAK | 2008-06-11 | View |
| 510(k) | K080271 | INREACH SYSTEM | JAK | 2008-03-31 | View |
| 510(k) | K071473 | MODIFICATION TO SUPERDIMENSION/BRONCHUS PREMIUM 2 | EOQ | 2007-07-12 | View |
| 510(k) | K062315 | SUPERDIMENSION/BRONCHUS PREMIUM 2 | JAK | 2006-09-08 | View |
| 510(k) | K052852 | SUPERDIMENSION/BRONCHUS PREMIUM | JAK | 2005-11-14 | View |
| 510(k) | K052260 | SUPERDIMENSION/BRONCHUS 4.1 | JAK | 2005-09-08 | View |
| 510(k) | K042438 | SUPERDIMENSION/BRONCHUS | JAK | 2004-11-08 | View |
No matching devices.
Advertisement