Kontron Instruments, Inc. - FDA 510(k) Cleared Devices
57
Total
57
Cleared
0
Denied
Kontron Instruments, Inc. has 57 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 57 cleared submissions from 1981 to 1993. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Kontron Instruments, Inc. Filter by specialty or product code using the sidebar.
57 devices
Cleared
Dec 15, 1993
MODIFICATIONS TO INTRA-AORTIC BALLOONS
Cardiovascular
259d
Cleared
Sep 27, 1993
MODIFICATION OF INTRA-AORTIC BALLOON CATHETERS
Cardiovascular
346d
Cleared
Mar 08, 1993
INTRA-AORTIC BALLOON PUMP CATHETER - MODIFICATION
Cardiovascular
249d
Cleared
Jun 19, 1991
KONTRON INTRA-AORTIC BALLOON PUMP, MODEL KAAT II
Cardiovascular
203d
Cleared
Jan 15, 1991
9.5 FR PERCUTANEOUS DB LUMEN 40CC FLEXI-CATH (TM)
Cardiovascular
174d
Cleared
Dec 03, 1990
KONTRON SIGMA 44 HVCD ULTRASOUND IMAGING SYSTEM
Cardiovascular
389d
Cleared
Sep 14, 1990
9.5F PERCU DOUBLE LUMEN INTRA-AORTIC BALLOON
Cardiovascular
529d
Cleared
Jan 26, 1990
SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283
Cardiovascular
561d
Cleared
Dec 13, 1989
MINIMON 7133B PATIENT MONITOR
Cardiovascular
37d
Cleared
Dec 12, 1989
KONTRON KOLORMON 7250 PATIENT MONITOR
Cardiovascular
34d
Cleared
Sep 26, 1989
MINIMON 7137B PATIENT MONITOR
Anesthesiology
19d
Cleared
Sep 20, 1989
10 FR PERCUTAN DOUBLE LUMEN INTRA-AORTIC BALLOON
Cardiovascular
156d
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