DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A— 510(k) K090742

Name: FDA 510(k) clearance K090742
Creator: U.S. Food and Drug Administration
Published: 2009-09-18

Substantially Equivalent

Samsung Mobile Display Co., Ltd.

FDA 510(k) clearance K090742 for DIGITAL FLAT PANEL X-RAY DETECTOR, MODEL LTX240AA01-A, Substantially Equivalent on 2009-09-18. Applicant: Samsung Mobile Display Co., Ltd.. Device class: 2.

Clearance details

Applicant: Samsung Mobile Display Co., Ltd.
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2009-03-20
Decision date: 2009-09-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Houston, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MQB

view all

K253800 — 0909FCE, 0909FCE-HS2026-07-31
K260820 — VIVIX-S 4386W (FXRD-4386WA)2026-06-18
K252996 — Universal 1417PI2026-06-12
K252911 — Lux HD 2530 detector (Lux HD 2530)2025-10-09
K250211 — Yushan X-Ray Flat Panel Detector2025-07-22

More clearances from Samsung Mobile Display Co., Ltd.

view all

K112751 — SDX-4343CS2011-11-23
K112558 — DIGITAL FLAT PANEL X-RAY DETECTOR2011-11-10
K102321 — DIGITAL FLAT PANEL X-RAY DETECTOR MODEL SDX-4336CP2011-02-11
K102587 — LLX240AB012010-12-01

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