FDA 510(k) Applications Submitted by DEBRA COGAN
| 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. |
| K212324 |
07/26/2021 |
RenovoCath |
RenovoRx, 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. |
| K223891 |
12/27/2022 |
Cobra Catheter System |
Endovascular Engineering |
|
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