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)

CENTRICITY UNIVERSAL VIEWER ZERO FOOTPRINT CLIENT

K-Number: K131977 · 2013-09-17

ApplicantGE Healthcare
Decision Date2013-09-17
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CENTRICITY UNIVERSAL VIEWER ZERO FOOTPRINT CLIENT is the device name listed in this FDA 510(k) record. The listed applicant is GE Healthcare. It received FDA 510(k) clearance on 2013-09-17 under 510(k) number K131977. 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 CENTRICITY UNIVERSAL VIEWER ZERO FOOTPRINT CLIENT?

CENTRICITY UNIVERSAL VIEWER ZERO FOOTPRINT CLIENT is a medical device that received FDA 510(k) clearance on 2013-09-17. The listed applicant is GE Healthcare. The 510(k) number is K131977.

When did CENTRICITY UNIVERSAL VIEWER ZERO FOOTPRINT CLIENT receive FDA 510(k) clearance?

CENTRICITY UNIVERSAL VIEWER ZERO FOOTPRINT CLIENT received FDA 510(k) clearance on 2013-09-17, under 510(k) number K131977.

Who is the listed applicant for CENTRICITY UNIVERSAL VIEWER ZERO FOOTPRINT CLIENT?

The FDA 510(k) record lists GE Healthcare as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTRICITY UNIVERSAL VIEWER ZERO FOOTPRINT CLIENT?

The FDA product code for CENTRICITY UNIVERSAL VIEWER ZERO FOOTPRINT CLIENT 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 GE Healthcare 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.

K253639ViewK242925MR Contour DLK232346Digital Expert Access with Remote ScanningK223212Precision DLK221680Xeleris V Processing and Review SystemK221932Omni Legend

View all 152 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.

↑