Telectronics, Inc. - FDA 510(k) Cleared Devices
107
Total
107
Cleared
0
Denied
Telectronics, Inc. has 107 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 107 cleared submissions from 1977 to 1990.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
107 devices
Cleared
Mar 06, 1990
IMPLANTABLE ADAPTOR 033-380
Cardiovascular
377d
Cleared
Sep 12, 1989
OPTIMA MPT AND SPT PACEMAKERS
Cardiovascular
189d
Cleared
Feb 02, 1989
VS-1 SILICONE IMPLANT LEADS (NEW SERIAL # TUBE)
Cardiovascular
86d
Cleared
Jan 26, 1989
OPTIMA MPT AND SPT PACEMAKERS
Cardiovascular
98d
Cleared
Dec 15, 1988
IMPLANTABLE ELECTRODE LEADS 033-400,402 AND 436
Cardiovascular
64d
Cleared
Jul 18, 1988
OPTIMA MPT SERIES III PACEMAKER, 5281D AND 5282D
Cardiovascular
77d
Cleared
May 31, 1988
IMPLANTABLE ELECTRODE LEAD, MODEL 030-446
Cardiovascular
200d
Cleared
Dec 17, 1987
MODEL 1740 PERSONAL POCKET PROGRAMMER
Cardiovascular
379d
Cleared
Nov 04, 1987
IMPLANTABLE PROGRAMMABLE CARDIAC PULSE GENERATORS
Cardiovascular
113d
Cleared
Aug 18, 1987
SLIMLINE UNIPOLAR ENDOCARDIAL PACING LEAD, 030-438
Cardiovascular
231d
Cleared
Aug 12, 1987
IMPLANTABLE PROGRAMMABLE CARDIAC PULSE GENERATORS
Cardiovascular
78d
Cleared
Jun 24, 1987
MODEL 5600B PROGRAMMER, PACEMAKER
Cardiovascular
33d
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