Icor AB - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Icor AB has 16 FDA 510(k) cleared anesthesiology devices. Based in Bromma, SE.
Historical record: 16 cleared submissions from 1986 to 1996.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
16 devices
Cleared
May 22, 1996
ET-TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)
Anesthesiology
245d
Cleared
Sep 07, 1995
TYPE 1 & 2 (HUMIDAIR I & II)
Anesthesiology
43d
Cleared
Jul 31, 1995
ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)
Anesthesiology
74d
Cleared
Jul 13, 1995
FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT...
Anesthesiology
23d
Cleared
Aug 15, 1994
HEAT AND MOISTURE EXCHANGERS AND FILTERS
Anesthesiology
112d
Cleared
Jul 27, 1994
COLIBRI
Anesthesiology
204d
Cleared
Jun 08, 1994
AFH, AFH FLEX, AFH/T, AFH/T FLEX, AF
Anesthesiology
76d
Cleared
May 26, 1993
FHB, FHB-T, FHBFLEX, FHBFLEX-T
Anesthesiology
201d
Cleared
Jun 23, 1992
BREATH-EASY, MODIFICATION
Ophthalmic
272d
Cleared
Dec 04, 1990
ICOR HCH 4, ICOR HCH 7
Anesthesiology
75d
Cleared
Jan 25, 1990
HCH 9165, 9165 S, 9166, HFH, HFH-T HEAT MOISTURE
Anesthesiology
14d
Cleared
Jan 04, 1990
ICOR CMU Q PLUS
Anesthesiology
85d
Cleared
Nov 04, 1988
ICOR AGENT MONITOR
Anesthesiology
78d
Cleared
May 17, 1988
BREATH-EASY
Anesthesiology
50d
Cleared
Sep 04, 1987
ICOR NEONATAL HCH
Anesthesiology
77d
Cleared
Mar 27, 1986
ICOR CALARIC MEASUREMENT UNIT (CMU)
Anesthesiology
107d