Diagnocat— 510(k) K252934

Substantially Equivalent

DGNCT, LLC

FDA 510(k) clearance K252934 for Diagnocat, Substantially Equivalent on 2026-01-15. Applicant: DGNCT, LLC. Device class: 2.

Clearance details

Applicant: DGNCT, LLC
Product code: Code MYN
Device class: Class 2
Regulation: 21 CFR 892.2070
Advisory panel: Radiology
Date received: 2025-09-15
Decision date: 2026-01-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami, FL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.