# Icor AB

- Location (FDA's records): Bromma, SE
- FDA decisions: 16 (1986–1996): 16 510(k) clearances
- Product codes: BYD (9), BZL (2), CCK (2), BTR (1), CBQ (1), HME (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K954402: ET-Tube Placement Detector (with Colibri Indicator) (May 22, 1996)
- K953507: Type 1 & 2 (Humidair I & II) (Sep 7, 1995)
- K952325: ET Tube Placement Detector (with Colibri Indicator) (Jul 31, 1995)
- K952823: FHB, FHB-T with or Without Flextube HFH, HFH-T, Afa, Afh-T with or Without Flexrtube (Jul 13, 1995)
- K941987: Heat and Moisture Exchangers and Filters (Aug 15, 1994)
- K940041: Colibri (Jul 27, 1994)
- K941436: Afh, Afh Flex, Afh/T, Afh/T Flex, AF (Jun 8, 1994)
- K925622: FHB, FHB-T, Fhbflex, Fhbflex-T (May 26, 1993)

Source page: https://510kreport.com/company/icor