Intermedics, Inc. - FDA 510(k) Cleared Devices
211
Total
201
Cleared
0
Denied
Intermedics, Inc. has 201 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 201 cleared submissions from 1977 to 1996.
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 - Intermedics, Inc.
211 devices
Not Cleared
Dec 16, 1996
MODEL 430-07 ENDOCARDIAL PACING LEAD
Cardiovascular
439d
Cleared
Nov 04, 1996
INTERMEDICS MODEL 436-07 BIPOLAR & MODEL 437-07 UNIPOLAR IMPLANTABLE...
Cardiovascular
361d
Cleared
Aug 21, 1996
BIPLR IM EN PAC LEADS (430-07,432-03,436-02 & 07, 438-05 & 07)
Cardiovascular
77d
Cleared
Jun 19, 1996
CARDIFIX EZ BIPOLAR/UNIPOLAR ENDOCARDIAL PACING LEAD
Cardiovascular
197d
Cleared
Jun 18, 1996
IMPLANTABLE PACING LEADS/IMPLANTABLE ACCESSORY/NON-IMPLANTABLE ACCESSORY
Cardiovascular
151d
Cleared
Feb 27, 1996
INTERMEDICS MODEL 430-07 BIPOLAR IMPLANTABLE ENDOCARDIAL PACING LEAD
Cardiovascular
137d
Cleared
Mar 15, 1995
INTERMEDICS TRIANGLE CHEST PROBE MODEL 526-04
Cardiovascular
624d
Cleared
Apr 29, 1993
CARDIFIX ENDOCARDIAL PACING LEAD
Cardiovascular
363d
Cleared
Jan 22, 1993
MODELS 438-05 AND 435-05 IMPLANTABLE PACING LEAD
Cardiovascular
217d
Cleared
Mar 17, 1992
INTERMEDICS MODEL 366-15 VS 1 HEADER PLUG
Cardiovascular
41d
Cleared
Sep 18, 1991
MODELS 432-03 & 433-03 IMPLANT ENDOCARD PAC LEAD
Cardiovascular
127d
Cleared
May 16, 1991
8MM QUANTUM PULSE/SUPRIMA II PULSE GENERATORS
Cardiovascular
65d
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