FDA 510(k) clearance · back to tracker

Derma-2

Neko Health AB cleared K253911 on 2026-05-20, decision: substantially equivalent

K-number

K253911

Sponsor

Neko Health AB

Device

Derma-2

Class

Class I

Decision

Substantially Equivalent

Decision date

2026-05-20

Product code

LHQ

Advisory committee

Obstetrics/Gynecology

Medical specialty

Obstetrics/Gynecology

Regulation number

884.2980

Official FDA record

Open K253911on 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 K253911 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.

Try the sandbox

Source

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