K830251 is an FDA 510(k) clearance for the CAMPY BLOOD AGAR PLATE. Classified as Culture Media, Selective And Differential (product code JSI), Class I - General Controls.
Submitted by Granite Diagnostics, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 28, 1983 after a review of 34 days - a notably fast clearance cycle.
This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.2360 - the FDA microbiology 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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