FDA 510(k) Applications Submitted by ARSTASIS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K121521 |
05/23/2012 |
AXERA ACCESS SYSTEM |
ARSTASIS, INC. |
| K151877 |
07/09/2015 |
MicroTract Access System |
ARSTASIS, INC. |
| K132263 |
07/22/2013 |
AXERA 2 ACCESS SYSTEM |
ARSTASIS, INC. |
| K102728 |
09/22/2010 |
ARSTASIS ACCESS SYSTEM |
ARSTASIS, INC. |
| K123135 |
10/05/2012 |
AXERA 2 ACCESS SYSTEM MODEL AXE200 |
ARSTASIS, INC. |
| K113110 |
10/20/2011 |
AXERA ACCESS SYSTEM |
ARSTASIS, INC. |
| K103143 |
10/25/2010 |
ARSTASIS ONE LATCHWIRE ACCESS SYSTEM |
ARSTASIS, INC. |
| K103421 |
11/22/2010 |
ARSTASIS DILATOR ADAPTER |
ARSTASIS, INC. |
| K123618 |
11/23/2012 |
AXERA 2 ACCESS SYSTEM |
ARSTASIS, INC. |
| K091006 |
04/08/2009 |
ITG VASCULAR ACCESS SYSTEM, MODEL 300 |
ARSTASIS, INC. |
| K140201 |
01/27/2014 |
AXERA 2 ACCESS SYSTEM |
ARSTASIS, INC. |
| K140287 |
02/05/2014 |
AXERA RX ACCESS SYSTEM |
ARSTASIS, INC. |
| K140871 |
04/04/2014 |
AXERA 2 ACCESS SYSTEM |
ARSTASIS, INC. |
| K100615 |
03/04/2010 |
ARSTASIS ACCESS SYSTEM |
ARSTASIS, INC. |
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