FDA 510(k) Applications for Medical Device Product Code "HCA"
(Catheter, Ventricular)
FDA 510(k) Number |
Applicant |
Device Name |
Decision Date |
K020728 |
AESCULAP, INC. |
MIETHKE SHUNT SYSTEM |
04/05/2002 |
K021481 |
BRESAGEN, INC. |
BRESAGEN CATHETER, MODEL CS-3000 |
08/06/2002 |
K031123 |
Codman & Shurtleff, Inc. |
CODMAN BACTISEAL BARIUM STRIPED CATHETERS |
05/14/2003 |
K003322 |
Codman & Shurtleff, Inc. |
CODMAN BACTISEAL CATHETERS |
10/01/2001 |
K992796 |
IMAGE-GUIDED NEUROLOGICS, INC. |
ASPIRATION/IRRIGATION CATHETER, MODEL AC-1000 |
10/25/1999 |
K013005 |
INNERSPACE, INC. |
ACT 11 MP VENTRICULAR CATHETER |
03/08/2002 |
K983331 |
MEDTRONIC PS MEDICAL |
MEDTRONIC PS MEDICAL INNERVISION VENTRICULAR CATHETER, 15CM MODEL 99102 |
12/16/1998 |
K123605 |
MRI INTERVENTIONS, INC. |
SMARTFLOW CATHETER |
08/16/2013 |
K161731 |
Parker Hannifin Corp. |
Cleveland Multiport Ventricular Catheter Set |
03/27/2017 |
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