K955897 is an FDA 510(k) clearance for the CRYPTO/GIARDIA-CEL IF TEST. Classified as Giardia Spp. (product code MHI), Class II - Special Controls.
Submitted by Techlab, Inc. (Blacksburg, US). The FDA issued a Cleared decision on August 5, 1996 after a review of 223 days — an extended review cycle.
This device falls under the Microbiology FDA review panel, regulated under 21 CFR 866.3220 — 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.