K844044 is an FDA 510(k) clearance for the LYTETEK 1000 NA/K SODIUM/POTASSIUM ANALYZER. Classified as Electrode, Ion Specific, Potassium (product code CEM), Class II - Special Controls.
Submitted by Medica Corp. (Newtonville, US). The FDA issued a Cleared decision on November 27, 1984 after a review of 41 days - a notably fast clearance cycle.
This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1600 - 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.
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