FDA 510(k) Applications Submitted by Susan Christensen
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K090148 |
01/21/2009 |
PROGUIDE CHRONIC DIALYSIS CATHETER |
MERIT MEDICAL SYSTEMS, INC. |
| K140513 |
02/28/2014 |
MERIT SAFETY INTRODUCER NEEDLE |
MERIT MEDICAL SYSTEMS, INC. |
| K180723 |
03/19/2018 |
PreludeSYNC DISTAL Radial Compression System |
Merit Medical Systems, Inc |
| K141363 |
05/23/2014 |
CENTROS LONG TERM HEMODIALYSIS CATHETER, CENTROSFLO LONG TERM HEMODIALYSIS CATHETER |
MERIT MEDICAL SYSTEMS, INC. |
| K091584 |
06/02/2009 |
MERIT MAK (MINI ACCESS KIT) WITH PALLADIUM TIP GUIDE WIRE |
MERIT MEDICAL SYSTEMS, INC. |
| K132155 |
07/12/2013 |
Merit ASAPLP Aspiration Catheter |
MERIT MEDICAL SYSTEMS, INC. |
| K151967 |
07/16/2015 |
Centros Long-Term Hemodialysis Catheter, CentrosFLO Long-Term Hemodialysis Catheter |
Merit Medical Systems, Inc. |
| K092303 |
07/29/2009 |
MERIT LAUREATE HYDROPHILIC GUIDE WIRE |
MERIT MEDICAL SYSTEMS, INC. |
| K172637 |
09/01/2017 |
HeRO Graft |
Merit Medical Systems, Inc. |
| K213845 |
12/09/2021 |
HeRO Graft |
Merit Medical Systems, Inc. |
| K203724 |
12/21/2020 |
HeRO Graft, HeRO Adapter |
Merit Medical Systems, Inc. |
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