K790456 is an FDA 510(k) clearance for the SERIES 7000. Classified as Gas-machine, Anesthesia (product code BSZ), Class II - Special Controls.
Submitted by Narco Mckesson Co. (Walker, US). The FDA issued a Cleared decision on March 23, 1979 after a review of 17 days - a notably fast clearance cycle.
This device falls under the Anesthesiology FDA review panel, regulated under 21 CFR 868.5160 - 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.
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