LIBERTY GLOBAL, LLC

FDA Device Registration & Listing · Scottsdale, AZ, US · Registration 3027373189

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3027373189
FEI Number
3027373189
Entity Name
LIBERTY GLOBAL, LLC
City/State/Country
Scottsdale, AZ, US
Establishment Address
7160 E. Kierland Blvd, Scottsdale, AZ 85254, US
Establishment Type(s)
Repack or Relabel Medical Device
Owner / Operator
Liberty Global, LLC (Owner Number: 10088126)
Owner / Operator Contact Address
7160 E. Kierland Blvd, Scottsdale, AZ 85254, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
K111551
PMA Number
N/A

All Registered Proprietary Names

GE Innova IGS360 Cath Lab Siemens Artis Zee Cath Lab OEC 9900 C Arm Philips FD20 Cath Lab GE OEC 9800 C arm

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IZI System, X-Ray, Angiographic Radiology Class 2 892.1600 2023-10-18
OWB Interventional Fluoroscopic X-Ray System Radiology Class 2 892.1650 2023-10-18
JAA System, X-Ray, Fluoroscopic, Image-Intensified Radiology Class 2 892.1650 2023-10-18
JAK System, X-Ray, Tomography, Computed Radiology Class 2 892.1750 2024-01-18
IZI System, X-Ray, Angiographic Radiology Class 2 892.1600 2024-01-18
OWB Interventional Fluoroscopic X-Ray System Radiology Class 2 892.1650 2024-01-18
JAA System, X-Ray, Fluoroscopic, Image-Intensified Radiology Class 2 892.1650 2024-01-18
OXO Image-Intensified Fluoroscopic X-Ray System, Mobile Radiology Class 2 892.1650 2023-06-28
OWB Interventional Fluoroscopic X-Ray System Radiology Class 2 892.1650 2023-06-28
JAA System, X-Ray, Fluoroscopic, Image-Intensified Radiology Class 2 892.1650 2023-06-28
JAA System, X-Ray, Fluoroscopic, Image-Intensified Radiology Class 2 892.1650 2023-06-28
IZI System, X-Ray, Angiographic Radiology Class 2 892.1600 2023-06-28
OWB Interventional Fluoroscopic X-Ray System Radiology Class 2 892.1650 2023-06-28
JAA System, X-Ray, Fluoroscopic, Image-Intensified Radiology Class 2 892.1650 2023-10-18
OXO Image-Intensified Fluoroscopic X-Ray System, Mobile Radiology Class 2 892.1650 2023-10-18
OWB Interventional Fluoroscopic X-Ray System Radiology Class 2 892.1650 2023-10-18

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Liberty Global, LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K163715 Philips Medical Systems Nederland B.V. Allura Xper R9 2017-01-26
K863853 Superior Medical Products EAZY COVERS 1987-03-06
K953974 Medivision Medical Imaging, Ltd. CAMVISION 1000 1996-09-09
K024012 Ge Oec Medical Systems OEC 9800 E/CV+ DIGITAL MOBILE IMAGING SYSTEM 2003-03-20
K970608 Guidant Cardiac and Vascular Surgery EVT MARKER BOARD 1997-04-21

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0001-2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands 2
Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
Z-0002-2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands 2
Allura Xper FD10; Model Numbers: (1) 722003, (2) 722010, (3) 722026; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
Z-0003-2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands 2
Allura Xper FD10/10; Model Numbers: (1) 722005, (2) 722011, (3) 722027; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
Z-0004-2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands 2
Allura Xper FD10 OR Table; Model Numbers: 722033; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;
Z-0005-2026 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands 2
Allura Xper FD20; Model Numbers: (1) 722006, (2) 722012, (3) 722028; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3027373189. Last updated year: 2026. Please use registration number 3027373189 when referencing this establishment in official correspondence.
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