K844781 is an FDA 510(k) clearance for the MEMBRANE KITS-KC1, CO2 & 02 FOR INSTRUMENT-LAB. Classified as Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph (product code CHL), Class II - Special Controls.
Submitted by Shaban Mfg. Co. (Fort Myers, US). The FDA issued a Cleared decision on February 1, 1985 after a review of 53 days - a notably fast clearance cycle.
This device falls under the Chemistry FDA review panel, regulated under 21 CFR 862.1120 - 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 Shaban Mfg. Co. devices