Arterys MICA— 510(k) K192437

Substantially Equivalent

Arterys, Inc.

FDA 510(k) clearance K192437 for Arterys MICA, Substantially Equivalent on 2020-03-25. Applicant: Arterys, Inc.. Device class: 2.

Clearance details

Applicant: Arterys, Inc.
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2019-09-06
Decision date: 2020-03-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Francisco, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code QIH

K260879 — 4DM2026-09-10
K261795 — Quicktome Software Suite2026-09-10
K251417 — ReVISION 22026-09-09
K260525 — NextMR Spine2026-09-04
K260811 — Heartvue.Proton2026-08-26

More clearances from Arterys, Inc.

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