Arstasis, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K132263 | AXERA 2 ACCESS SYSTEM | DYB | 2013-08-19 | View |
| 510(k) | K123618 | AXERA 2 ACCESS SYSTEM | DYB | 2013-03-24 | View |
| 510(k) | K123135 | AXERA 2 ACCESS SYSTEM MODEL AXE200 | DYB | 2013-01-28 | View |
| 510(k) | K121521 | AXERA ACCESS SYSTEM | DYB | 2012-06-21 | View |
| 510(k) | K113110 | AXERA ACCESS SYSTEM | DYB | 2011-11-09 | View |
| 510(k) | K103421 | ARSTASIS DILATOR ADAPTER | DRE | 2011-05-24 | View |
| 510(k) | K103143 | ARSTASIS ONE LATCHWIRE ACCESS SYSTEM | DYB | 2011-02-02 | View |
| 510(k) | K102728 | ARSTASIS ACCESS SYSTEM | DYB | 2010-10-07 | View |
| 510(k) | K100615 | ARSTASIS ACCESS SYSTEM | DYB | 2010-03-30 | View |
| 510(k) | K091006 | ITG VASCULAR ACCESS SYSTEM, MODEL 300 | DYB | 2010-02-25 | View |
No matching devices.
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