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)

JUSHA-M52C MEDICAL DISPLAY

K-Number: K131390 · 2013-11-27

ApplicantNanjing Jusha Display Technology Co., Ltd.
Decision Date2013-11-27
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

JUSHA-M52C MEDICAL DISPLAY is the device name listed in this FDA 510(k) record. The listed applicant is Nanjing Jusha Display Technology Co., Ltd.. It received FDA 510(k) clearance on 2013-11-27 under 510(k) number K131390. 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 JUSHA-M52C MEDICAL DISPLAY?

JUSHA-M52C MEDICAL DISPLAY is a medical device that received FDA 510(k) clearance on 2013-11-27. The listed applicant is Nanjing Jusha Display Technology Co., Ltd.. The 510(k) number is K131390.

When did JUSHA-M52C MEDICAL DISPLAY receive FDA 510(k) clearance?

JUSHA-M52C MEDICAL DISPLAY received FDA 510(k) clearance on 2013-11-27, under 510(k) number K131390.

Who is the listed applicant for JUSHA-M52C MEDICAL DISPLAY?

The FDA 510(k) record lists Nanjing Jusha Display Technology Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for JUSHA-M52C MEDICAL DISPLAY?

The FDA product code for JUSHA-M52C MEDICAL DISPLAY 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 Nanjing Jusha Display Technology Co., 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.

K230728JUSHA-C810G/C810G LCD Monitor, JUSHA-C660/JUSHA-C660G/C660/C660G LCD MonitorK231170C350/C350G LCD Monitor; M550/M550G LCD MonitorK230723C510G/JUSHA-C510G/C510/JUSHA- C510 LCD MonitorK230643CP620G LCD monitor, CP620 LCD monitorK222121C630G LCD monitor, JUSHA-C630G LCD monitor, C630 LCD monitor, JUSHA-C630 LCD monitorK212231C1210G LCD Monitor, JUSHA-C1210G LCD Monitor, C1210 LCD Monitor, JUSHA-C1210 LCD Monitor

View all 18 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.

↑