FDA 510(k) Applications Submitted by MICHAEL J BILLIG
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K992833 |
08/23/1999 |
VACUUM ASSIST STABILIZER |
CARDIO THORACIC SYSTEMS |
| K955551 |
12/05/1995 |
CARDI0METRICS FLOW WIRE XT DOPPLER GUIDE MODEL 1403, 1404 |
CARDIOMETRICS, INC. |
| K970638 |
02/20/1997 |
CTS MIDCAB FIXEDN DIAMETER CORONARY SHUNT |
CARDIOTHORACIC SYSTEMS, INC. |
| K070485 |
02/20/2007 |
BOOMERANG WIRE /BOOMERANG PLUS WIRE SYSTEM, MODEL# B PLUS WIRE 58L |
CARDIVA MEDICAL, INC. |
| K991073 |
03/31/1999 |
ACIER SUTURES |
CARDIO THORACIC SYSTEMS |
| K951567 |
04/04/1995 |
CARDIOMETICS FLOWIRE, SMARTWIRE DOPPLER GUIDE WIRE |
CARDIOMETRICS, INC. |
| K111493 |
05/31/2011 |
NIDEK MULTICOLOR SCAN LASER PHOTOCOAGULATOR MC-500 VIXI |
NIDEK CO., LTD. |
| K062192 |
07/31/2006 |
OSTIAL PRO STENT POSITIONING SYSTEM |
OSTIAL SOLUTIONS, LLC |
| K963503 |
09/03/1996 |
CTS MIDCAB CORONARY SHUNT |
CARDIOTHORACIC SYSTEMS, INC. |
| K963930 |
10/01/1996 |
CTS MIDCAB/SVH BIPOLAR SCISSORS |
CARDIOTHORACIC SYSTEMS, INC. |
| K963965 |
10/02/1996 |
CTS MIDCAB STITCHER |
CARDIOTHORACIC SYSTEMS, INC. |
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