FDA 510(k) Applications Submitted by TIFFINI DIAGE
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K121083 |
04/10/2012 |
TRUE DILATATION PERCUTANEOUS TRANSLUMINAL VALVULOPLASTY CATHETER, 20MM X 4.5CM, TRUE DILATATION PERCUTANEOUS TRANSLUMINA |
LOMA VISTA MEDICAL |
| K141119 |
04/30/2014 |
CAMERA ENABLED PROBE |
TRICE MEDICAL, INC. |
| K162475 |
09/06/2016 |
mi-eye 2, mi-eye 2 monitor |
Trice Medical |
| K152789 |
09/25/2015 |
FLEX SCORING CATHETER |
VENTUREMED GROUP |
| K152924 |
10/05/2015 |
TIVA┐ |
VELANO VASCULAR |
| K142946 |
10/10/2014 |
TIVA |
Velano Vascular, Inc. |
| K133569 |
11/20/2013 |
TRUE DILATATION BALLOON VALVULOPLASTY CATHETER, 20MM X 4.5 CM, 22MM X 4.5CM, 24 MM X 4.5CM, 26MM X 4.5CM |
BARD PERIPHERAL VASCULAR, INC. |
| K163508 |
12/14/2016 |
PIVO |
Velano Vascular |
|
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