K952823 is an FDA 510(k) clearance for the FHB, FHB-T WITH OR WITHOUT FLEXTUBE HFH, HFH-T, AFA, AFH-T WITH OR WITHOUT FL.... Classified as Condenser, Heat And Moisture (artificial Nose) (product code BYD), Class I - General Controls.
Submitted by Icor AB (Bromma, SE). The FDA issued a Cleared decision on July 13, 1995 after a review of 23 days - a notably fast clearance cycle.
This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5375 - the FDA anesthesiology and respiratory device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.
Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.
View all Icor AB devices