K884731 is an FDA 510(k) clearance for the LYTENING 6 SODIUM/POTASSIUM/IONIZED CALCIUM ANALYZ. Classified as Electrode, Ion Specific, Calcium (product code JFP), Class II - Special Controls.
Submitted by Amdev, Inc. (Danvers, US). The FDA issued a Cleared decision on February 3, 1989 after a review of 85 days - a notably fast clearance cycle.
This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1145 - the FDA in vitro diagnostics and chemistry 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 Amdev, Inc. devices