FDA 510(k) Applications Submitted by LARRY SMITH
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K190789 |
03/27/2019 |
IntelliCartTM System |
Dornoch Medical Systems |
K080976 |
04/07/2008 |
NEXUS I.V. FLUID TRANSFER DEVICE |
NEXUS MEDICAL, LLC |
K081123 |
04/21/2008 |
NEXUS I.V. NEEDLESS ACCESS CANNULA FOR INTRAVASCULAR ADMINISTRATION SETS |
NEXUS MEDICAL, LLC |
K172481 |
08/16/2017 |
IntelliCart System |
Dornoch Medical Systems |
K162421 |
08/30/2016 |
IntelliCartTM System |
DORNOCH MEDICAL SYSTEMS |
K002724 |
08/31/2000 |
NUMALINK |
NUMA, INC. |
K123188 |
10/11/2012 |
DORNOCH DUO SUCTION CART WITH DL2800 LID MODEL UL-DU2800, DORNOCH DUO SUCTION CART WITH CL500 LID MODEL UL-DU500, DORNOC |
DORNOCH MEDICAL SYSTEMS, INC. |
K133786 |
12/12/2013 |
DORNOCH DUO SUCTION CART WITH: DL2800 LID, CL500 LID, DORNOCH QUAD SUCTION CART WITH: DL2800 LID, CL500 LID |
DORNOCH MEDICAL SYSTEMS, INC. |
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