Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwedenLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list ICOR AB with 16 510(k) clearances. The most recent is a 510(k) clearance dated May 22, 1996: ET-TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR).
| Date | Record | Source |
|---|---|---|
| May 22, 1996 | ET-TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)K954402 · CCK | 510(k) clearances |
| Sep 7, 1995 | TYPE 1 & 2 (HUMIDAIR I & II)K953507 · BYD | 510(k) clearances |
| Jul 31, 1995 | ET TUBE PLACEMENT DETECTOR (WITH COLIBRI INDICATOR)K952325 · CCK | 510(k) clearances |
| Jul 13, 1995 | FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT FLEXRTUBEK952823 · BYD | 510(k) clearances |
| Aug 15, 1994 | HEAT AND MOISTURE EXCHANGERS AND FILTERSK941987 · BYD | 510(k) clearances |
| Jul 27, 1994 | COLIBRIK940041 · BTR | 510(k) clearances |
| Jun 8, 1994 | AFH, AFH FLEX, AFH/T, AFH/T FLEX, AFK941436 · BYD | 510(k) clearances |
| May 26, 1993 | FHB, FHB-T, FHBFLEX, FHBFLEX-TK925622 · BYD | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
