FDA 510(k) clearance · back to tracker

Kneu Platform (V2)

Kneu Health Digital , Ltd. cleared K262515 on 2026-08-20, decision: substantially equivalent

K-number

K262515

Sponsor

Kneu Health Digital , Ltd.

Device

Kneu Platform (V2)

Class

Class II

Decision

Substantially Equivalent

Decision date

2026-08-20

Product code

GYD

Advisory committee

Neurology

Medical specialty

Neurology

Regulation number

882.1950

Official FDA record

Open K262515on 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

Drop K262515 into Compass and start a substantial-equivalence draft.

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.

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Source

Public 510(k) database, U.S. Food and Drug Administration, accessed via openFDA. Page refreshed weekly.