FDA 510(k) clearance · back to tracker
Oncomine Dx Express Test
Life Technologies Corporation cleared K260827 on 2026-10-15, decision: substantially equivalent
K-number
K260827
Sponsor
Life Technologies Corporation
Device
Oncomine Dx Express Test
Class
Class II
Decision
Substantially Equivalent
Decision date
2026-10-15
Product code
SBY
Advisory committee
Pathology
Medical specialty
Pathology
Regulation number
866.6085
Official FDA record
Open K260827on accessdata.fda.gov →
FDA's authoritative 510(k) summary page. Includes the decision letter, predicate references, and downloadable substantial-equivalence determination.
openFDA JSON
Raw record →
Machine-readable JSON. Useful for cross-referencing classification, product code, and advisory committee fields.
Use this as a predicate
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Compass pulls the predicate's intended use, technological characteristics, and performance data, maps them against your device, and produces a draft SE table aligned to FDA's 510(k) program guidance.
Try the sandboxSource
Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.