Cardiac Control Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Cardiac Control Systems, Inc. - FDA 510(k) Cleared Devices
26
Total
24
Cleared
0
Denied
Cardiac Control Systems, Inc. has 24 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 24 cleared submissions from 1983 to 1997.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Cardiac Control Systems, Inc.
26 devices
Cleared
Dec 29, 1997
INTERIM AV SHAPED TEMPORARY PACING CATHETER MODEL INT-AV610
Cardiovascular
230d
Cleared
May 15, 1995
CCDS MAESTRO(R) II SERIES 200 CADIAC PACEMAKER
Cardiovascular
146d
Cleared
May 03, 1995
CCS MAESTRO(R) II SERIES 200 MODELS 235 AND 227 CARDIAC PACEMAKER
Cardiovascular
104d
Cleared
May 14, 1993
CCS MAESTRO II SERIES 200 CARDIAC PACEMAKER
Cardiovascular
284d
Cleared
May 16, 1991
MAESTRO(R) SERIES 100/200 CARDIAC S/CHAMB PACEMAKE
Cardiovascular
136d
Cleared
Jan 03, 1991
MAESTRO SERIES 100/200 CARDIAC SINGLE CHAMBER PACE
Cardiovascular
63d
Cleared
Sep 26, 1989
MAESTRO PACEMAKER TEST MAGNET
Cardiovascular
42d
Cleared
Oct 17, 1988
MAESTRO(R) SERIES 100/200 SINGLE CHAMBER PACEMAKER
Cardiovascular
25d
Cleared
Oct 14, 1988
POLYSAFE(TM) IMPLANTABLE PACING LEAD
Cardiovascular
22d
Cleared
Oct 06, 1988
POLYSAFE IMPLANT. PACING LEADS W/TRABECULOK TIP
Cardiovascular
79d
Cleared
Sep 16, 1988
POLYSAFE IMPLANT. PACING LEADS W/TINED FIXA. TIP
Cardiovascular
59d
Cleared
Apr 11, 1988
MAESTRO(R) MODELS 115, 118, 215 AND 218 PACEMAKERS
Cardiovascular
76d