Coratomic, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Coratomic, Inc. - FDA 510(k) Cleared Devices
15
Total
14
Cleared
0
Denied
Coratomic, Inc. has 14 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1976 to 1986.
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 - Coratomic, Inc.
15 devices
Cleared
Oct 08, 1986
MODIFICATION OF STERILITY CYCLE PARAMETERS
Cardiovascular
36d
Cleared
Dec 15, 1982
CORATOMIC #VX5-105 & VX5-205 PULSE GEN.
Cardiovascular
91d
Cleared
Jun 22, 1982
C-101-P
Cardiovascular
77d
Cleared
May 28, 1982
CORATOMIC MODEL OVALITH 920BP
Cardiovascular
46d
Cleared
May 28, 1982
CORATOMIC MODEL OVALITH-920
Cardiovascular
45d
Cleared
May 15, 1981
CORATOMIC MODEL OVALITH-920
Cardiovascular
52d
Cleared
Oct 28, 1980
L-15T ENDOCARDIAL PACING ELECTRODE
Cardiovascular
Cleared
Feb 11, 1980
OVALITH P-BP BIPOLAR CARDIAC PACEMAKER
Cardiovascular
13d
Cleared
Jul 30, 1979
OVALITH-300
Cardiovascular
158d
Cleared
Dec 04, 1978
OVALITH 10BP
Cardiovascular
117d
Cleared
Jun 14, 1978
L-12, L-21, AND L-22 ELECTRODES
Cardiovascular
64d
Cleared
Feb 06, 1978
ENDOCARDIAL PACING ELECTRODE
Cardiovascular
59d
Cleared
Nov 02, 1977
L-501 CARDIAC PACEMAKER
Cardiovascular
12d
Cleared
Mar 28, 1977
C-L0L CARDIAC PACEMAKER
Cardiovascular
5d
Cleared
Dec 14, 1976
ENDO-LOK L-40 ENDOCARDIAL PACING ELECT.
Cardiovascular
80d