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Icor AB

FDA 510(k) & PMA Approved Devices — 16 products

Total Devices16
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K954402 ET-TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)CCK1996-05-22 View
510(k) K953507 TYPE 1 & 2 (HUMIDAIR I & II)BYD1995-09-07 View
510(k) K952325 ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)CCK1995-07-31 View
510(k) K952823 FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT FLEXRTUBEBYD1995-07-13 View
510(k) K941987 HEAT AND MOISTURE EXCHANGERS AND FILTERSBYD1994-08-15 View
510(k) K940041 COLIBRIBTR1994-07-27 View
510(k) K941436 AFH, AFH FLEX, AFH/T, AFH/T FLEX, AFBYD1994-06-08 View
510(k) K925622 FHB, FHB-T, FHBFLEX, FHBFLEX-TBYD1993-05-26 View
510(k) K914416 BREATH-EASY, MODIFICATIONHME1992-06-23 View
510(k) K904338 ICOR HCH 4, ICOR HCH 7BYD1990-12-04 View
510(k) K900150 HCH 9165, 9165 S, 9166, HFH, HFH-T HEAT MOISTUREBYD1990-01-25 View
510(k) K895935 ICOR CMU Q PLUSBZL1990-01-04 View
510(k) K883532 ICOR AGENT MONITORCBQ1988-11-04 View
510(k) K881308 BREATH-EASYBYD1988-05-17 View
510(k) K872371 ICOR NEONATAL HCHBYD1987-09-04 View
510(k) K854927 ICOR CALARIC MEASUREMENT UNIT (CMU)BZL1986-03-27 View
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