K024350 is an FDA 510(k) clearance for the ACON H. PYLORI RAPID TEST STRIP AND ACON H. PYLORI RAPID TEST DEVICE. Classified as Helicobacter Pylori (product code LYR), Class I - General Controls.
Submitted by ACON Laboratories, Inc. (San Diego, US). The FDA issued a Cleared decision on April 2, 2003 after a review of 93 days - within the typical 510(k) review window.
This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3110 - 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: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Microbiology review framework, consistent with the majority of Class II 510(k) submissions.
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