FDA 510(k) Applications Submitted by SABA MODJARRAD
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K090824 |
03/26/2009 |
BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) QX AMPLIFIED DNA ASSAY |
BECTON, DICKINSON & CO. |
| K090827 |
03/26/2009 |
BD PROBETEC NEISSERIA GONORRHOEAE (GC) QX AMPLIFIED DNA ASSAY |
BECTON, DICKINSON & CO. |
| K091724 |
06/11/2009 |
BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) Q AMPLIFIED DNA ASSAY |
BECTON DICKINSON & CO. |
| K091730 |
06/11/2009 |
BD PROBETEC NEISSERIA GONORRHOEAE (GC) QX AMPLIFIED DNA ASSAY |
BECTON, DICKINSON & CO. |
| K011881 |
06/18/2001 |
DYNALINK .035 BILIARY SELF-EXPANDING STENT SYSTEM |
GUIDANT CORP. |
| K012050 |
07/02/2001 |
VIATRAC 14 PLUS PERIPHERAL DILATATION CATHETER |
GUIDANT CORP. |
| K043023 |
11/03/2004 |
PRUITT-INAHARA OUTLYING CAROTID SHUNT, MODELS, 2012-49, 2013-49, 2014-49,2015-49,2016-49, 2017-49 |
LEMAITRE VASCULAR, INC. |
| K014007 |
12/05/2001 |
DYNALINK .018 BILLARY SELF-EXPANDING STENT SYSTEM |
GUIDANT CORP. |
| K014184 |
12/20/2001 |
MODIFICATION TO DYNALINK .035 BILIARY SELF-EXPANDING STENT SYSTEM |
GUIDANT CORP. |
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