MEDITECH EUROSCANNER M250— 510(k) K850027

Name: FDA 510(k) clearance K850027
Creator: U.S. Food and Drug Administration
Published: 1985-04-04

Substantially Equivalent

Stuart Medical, Inc.

FDA 510(k) clearance K850027 for MEDITECH EUROSCANNER M250, Substantially Equivalent on 1985-04-04. Applicant: Stuart Medical, Inc.. Device class: 2.

Clearance details

Applicant: Stuart Medical, Inc.
Product code: Code JAK
Device class: Class 2
Regulation: 21 CFR 892.1750
Advisory panel: Radiology
Date received: 1985-01-04
Decision date: 1985-04-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia, MD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JAK

view all

K253836 — FCT iStream Phase 22026-09-04
K253450 — BodyTom Elite (NL4000)2026-07-28
K253770 — CardIQ Suite2026-07-21
K253560 — Enhanced Boundary for PCCT2026-06-24
K253026 — Respiratory Gating for Scanners (2.1)2026-06-04

More clearances from Stuart Medical, Inc.

view all

K920294 — SMI MODEL 210 AMBULATORY ECG MONITORING SYSTEM1992-07-07

Adverse events under product code JAK

product code JAK

Death: 27
Injury: 571
Malfunction: 779
Total: 1,377

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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