K841183 is an FDA 510(k) clearance for the SODIUM CHLORIDE SOLUTION BLOOD CELL. Classified as Pad, Kelly (product code FNW), Class II - Special Controls.
Submitted by Reagent Laboratory, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 21, 1984 after a review of 62 days - a notably fast clearance cycle.
This device falls under the Hematology FDA review panel, regulated under 21 CFR 878.4370 - the FDA hematology 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 Reagent Laboratory, Inc. devices