FDA 510(k) Applications Submitted by SETH SCHULMAN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K122756 |
09/07/2012 |
PENUMBRA PUMP MAX (110VAC), PENUMBRA PUMP MAX (230VAC), PENUMBAR PUMP MAX CANISTER/TUBING |
PENUMBRA, INC. |
| K122772 |
09/10/2012 |
PENUMBRA DDC CATHETERS |
PENUMBRA, INC. |
| K132931 |
09/18/2013 |
APOLLO SYSTEM |
PENUMBRA, INC. |
| K113163 |
10/26/2011 |
PENUMBRA SYSTEM MAX |
PENUMBRA, INC. |
| K133317 |
10/28/2013 |
PENUMBRA SYSTEM / PENUMBRA SYSTEM MAX |
PENUMBRA, INC. |
| K000037 |
01/06/2000 |
MONOFILAMENT BIOSYN SUTURE |
UNITED STATES SURGICAL, A DIVISION OF TYCO HEALTHC |
| K100826 |
03/24/2010 |
PENUMBRA CATHERER 025 |
PENUMBRA, INC. |
| K012985 |
09/06/2001 |
MATRIX DETACHABLE COILS |
BOSTON SCIENTIFIC, TARGET |
| K103305 |
11/09/2010 |
PENUMBRA EMBOLIZATION COIL SYSTEM |
PENUMBRA, INC. |
| K014109 |
12/14/2001 |
IN-TIME RETRIEVAL DEVICE |
BOSTON SCIENTIFIC, TARGET |
| K093970 |
12/23/2009 |
PICA CATHETER |
PENUMBRA, INC. |
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