Data / Medical devices / United States / Liberty Global, LLC

Liberty Global, LLC: FDA-registered device maker in Scottsdale, AZ, United States, 7 510(k) clearances

Name: Liberty Global, LLC FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Liberty Global, LLC is registered with the FDA (registration 3027373189) in Scottsdale, AZ, United States. It lists 6 device types. The FDA files 7 510(k) clearances under its listings, the newest dated June 9, 2016. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3027373189
Address: 7160 E. Kierland Blvd, Scottsdale, AZ, United States, 85254
Owner or operator: Liberty Global, LLC (10088126)
Roles: Repackager or relabeler
First device listed: June 28, 2023
Registered through: 2026
Brand names listed: GE Innova IGS360 Cath Lab, GE Lightspeed VCT CT Scanner, GE OEC 9800 C arm, OEC 9900 C Arm, Optima MR450w 1.5T, Philips FD20 Cath Lab, Siemens Artis Zee Cath Lab

Devices it lists

Device	Product code	Class	Role	Source
Image-Intensified Fluoroscopic X-Ray System, Mobile	OXO	2	Repackager or relabeler	accessdata.fda.gov
Interventional Fluoroscopic X-Ray System	OWB	2	Repackager or relabeler	accessdata.fda.gov
System, Nuclear Magnetic Resonance Imaging	LNH	2	Repackager or relabeler	accessdata.fda.gov
System, X-Ray, Angiographic	IZI	2	Repackager or relabeler	accessdata.fda.gov
System, X-Ray, Fluoroscopic, Image-Intensified	JAA	2	Repackager or relabeler	accessdata.fda.gov
System, X-Ray, Tomography, Computed	JAK	2	Repackager or relabeler	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
June 9, 2016	K160618	Discovery MR750 3.0T, Discovery MR450 1.5T, Discovery MR750w 3.0T, Optima MR450w 1.5T	LNH	Substantially Equivalent	Ge Medical Systems, LLC	accessdata.fda.gov
September 5, 2014	K141574	ARTIS ZEE/ZEEGO SW VC21	OWB	Substantially Equivalent	Siemens Medical Solutions USA, Inc.	accessdata.fda.gov
January 2, 2013	K122457	GE INNOVA/INNOVA IGS/DISCOVERY IGS/OPTIMA ANGIOGRAPHIC, FLUOSCOPIC X-RAY SYSTEMS WITH CATHLAB FRONTIERS SOLUTIONS	OWB	Substantially Equivalent	GE Healthcare	accessdata.fda.gov
October 4, 2011	K111551	OEC(R) 9800, OEC(R) 9800 PLUS	OWB	Substantially Equivalent	Ge Oec Medical Systems, Inc.	accessdata.fda.gov
May 2, 2008	K073543	OEC 9900 ELITE	OWB	Substantially Equivalent	Ge Oec Medical Systems	accessdata.fda.gov
March 1, 2004	K040372	LIGHTSPEED 7.0 CT SCANNER SYSTEM	JAK	Substantially Equivalent	Ge Medical Systems, LLC	accessdata.fda.gov
December 9, 2003	K033737	ALLURA XPER FD20	OWB	Substantially Equivalent	Philips Medical Systems North America, Inc.	accessdata.fda.gov

Compare with other makers

Updated June 9, 2016. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.