Company ยท SE
Icor AB
FDA 510(k) clearances and medical device recalls filed under this name, 1986 to 1996. Name variants (Inc, Corp, punctuation) are merged.
16510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 22, 1996 | K954402 | ET-TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR) Icor AB, SE | CCK |
| Sep 7, 1995 | K953507 | TYPE 1 & 2 (HUMIDAIR I & II) Icor AB, SE | BYD |
| Jul 31, 1995 | K952325 | ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR) Icor AB, SE | CCK |
| Jul 13, 1995 | K952823 | FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT FLEXRTUBE Icor AB, SE | BYD |
| Aug 15, 1994 | K941987 | HEAT AND MOISTURE EXCHANGERS AND FILTERS Icor AB, SE | BYD |
| Jul 27, 1994 | K940041 | COLIBRI Icor AB, SE | BTR |
| Jun 8, 1994 | K941436 | AFH, AFH FLEX, AFH/T, AFH/T FLEX, AF Icor AB, SE | BYD |
| May 26, 1993 | K925622 | FHB, FHB-T, FHBFLEX, FHBFLEX-T Icor AB, SE | BYD |
| Jun 23, 1992 | K914416 | BREATH-EASY, MODIFICATION Icor AB, SE | HME |
| Dec 4, 1990 | K904338 | ICOR HCH 4, ICOR HCH 7 Icor AB, SE | BYD |
| Jan 25, 1990 | K900150 | HCH 9165, 9165 S, 9166, HFH, HFH-T HEAT MOISTURE Icor AB, SE | BYD |
| Jan 4, 1990 | K895935 | ICOR CMU Q PLUS Icor AB, SE | BZL |
| Nov 4, 1988 | K883532 | ICOR AGENT MONITOR Icor AB, SE | CBQ |
| May 17, 1988 | K881308 | BREATH-EASY Icor AB, SE | BYD |
| Sep 4, 1987 | K872371 | ICOR NEONATAL HCH Icor AB, SE | BYD |
| Mar 27, 1986 | K854927 | ICOR CALARIC MEASUREMENT UNIT (CMU) Icor AB, SE | BZL |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||