Icor AB
Icor AB holds FDA 510(k) medical device clearances, first cleared 1986, most recent 1996.
Top product codes for Icor AB
Recent clearances by Icor AB
- K954402 — ET-TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)
- K953507 — TYPE 1 & 2 (HUMIDAIR I & II)
- K952325 — ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)
- K952823 — FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT FLEXRTUBE
- K941987 — HEAT AND MOISTURE EXCHANGERS AND FILTERS
- K940041 — COLIBRI
- K941436 — AFH, AFH FLEX, AFH/T, AFH/T FLEX, AF
- K925622 — FHB, FHB-T, FHBFLEX, FHBFLEX-T
- K914416 — BREATH-EASY, MODIFICATION
- K904338 — ICOR HCH 4, ICOR HCH 7
- K900150 — HCH 9165, 9165 S, 9166, HFH, HFH-T HEAT MOISTURE
- K895935 — ICOR CMU Q PLUS
- K883532 — ICOR AGENT MONITOR
- K881308 — BREATH-EASY
- K872371 — ICOR NEONATAL HCH
- K854927 — ICOR CALARIC MEASUREMENT UNIT (CMU)
Data sourced from openFDA. This site is unofficial and independent of the FDA.