Kontron Instruments, Inc. - FDA 510(k) Cleared Devices
57
Total
57
Cleared
0
Denied
37 devices
Cleared
Oct 01, 1986
NOVEMPERC DOUBLE LUMEN INTRA-AORTIC BALLOON
Cardiovascular
223d
Cleared
May 07, 1986
KONTRON INTRA-AORTIC BALLOON PUMP MODEL KAAT
Cardiovascular
92d
Cleared
Jan 22, 1986
INTRA-AORTIC BALLOON PUMP MODEL K2000
Cardiovascular
187d
Cleared
Dec 04, 1985
KONTRON DEFIBRILLATOR 7501
Cardiovascular
40d
Cleared
Sep 20, 1985
KONTRON SIGMA ISC ECHOCARDIOGRAPH SYSTEM
Cardiovascular
98d
Cleared
May 16, 1985
KONTRON SUPERMON 7210 PATIENT MONITOR
Cardiovascular
163d
Cleared
Apr 04, 1985
KONTRON MINIMON 7134 PATIENT MONITOR
Cardiovascular
155d
Cleared
Mar 27, 1985
KONTRON MINIMON 7132 PATIENT MONITOR
Cardiovascular
113d
Cleared
Mar 27, 1985
KONTRON MINIMON 7131 PATIENT MONITOR
Cardiovascular
113d
Cleared
Aug 06, 1982
KONTRON LITWAK-KOFFSKY OBTURATED CANNU
Cardiovascular
94d
Cleared
Apr 29, 1982
ADAPTATION OF KANTRON 40 CC. PDLIAB
Cardiovascular
98d
Cleared
Sep 25, 1981
KONTRON PMS 7000
Cardiovascular
37d