Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MD213MC 21.3 DIAGNOSTIC IMAGING LCD MONITOR MODEL, L218TJ

K-Number: K090218 · 2009-04-15

ApplicantNec Display Solutions , Ltd.
Decision Date2009-04-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MD213MC 21.3 DIAGNOSTIC IMAGING LCD MONITOR MODEL, L218TJ is the device name listed in this FDA 510(k) record. The listed applicant is Nec Display Solutions , Ltd.. It received FDA 510(k) clearance on 2009-04-15 under 510(k) number K090218. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MD213MC 21.3 DIAGNOSTIC IMAGING LCD MONITOR MODEL, L218TJ?

MD213MC 21.3 DIAGNOSTIC IMAGING LCD MONITOR MODEL, L218TJ is a medical device that received FDA 510(k) clearance on 2009-04-15. The listed applicant is Nec Display Solutions , Ltd.. The 510(k) number is K090218.

When did MD213MC 21.3 DIAGNOSTIC IMAGING LCD MONITOR MODEL, L218TJ receive FDA 510(k) clearance?

MD213MC 21.3 DIAGNOSTIC IMAGING LCD MONITOR MODEL, L218TJ received FDA 510(k) clearance on 2009-04-15, under 510(k) number K090218.

Who is the listed applicant for MD213MC 21.3 DIAGNOSTIC IMAGING LCD MONITOR MODEL, L218TJ?

The FDA 510(k) record lists Nec Display Solutions , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MD213MC 21.3 DIAGNOSTIC IMAGING LCD MONITOR MODEL, L218TJ?

The FDA product code for MD213MC 21.3 DIAGNOSTIC IMAGING LCD MONITOR MODEL, L218TJ is LLZ.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Nec Display Solutions , Ltd. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K161057Diagnostic Imaging Color LCD MonitorK130772MD211C2 21.3 DIAGNOSTIC IMAGING LCD MONITORK130770MD211C3 21.3 DIAGNOSTIC IMAGING LCD MONITORK111237MD301C4 29.8 DIAGNOSTIC IMAGING LCD MONITOR, L309TYK090215MD213MG 21.3 DIAGNOSTIC IMAGING LCD MONITOR - L218TLK083916LCD3090WQXI OR MD304MC 29.8 INCH DIAGNOSTIC IMAGING LCD MONITOR, MODEL L307TD

View all 12 devices →

Related Devices (Code: LLZ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261874Syneris PACS v.1.0.1.0SynerisK262442HipStudio AnalysisReplasia BVK261855Elucid PlaqueIQElucid Bioimaging, Inc.K254214OOOPDSTaiwan Main Orthopaedic Biotechnology Co., Ltd.K261861SPINEsim v1.0Mdsim S.A.K2620603D-RD-SRadiopharmaceutical Imaging & Dosimetry, LLC

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑