510(k) K161563

Device
Allura Xper FD Series And Allura Xper OR Table Series
Applicant
Philips Medical Systems Nederland BV
510(k) number
K161563
Product code
OWB  
Decision
Substantially Equivalent (SESE)
Decision date
2016-07-29
Date received
2016-06-06
Regulation
892.1650
Classification name
Interventional Fluoroscopic X-ray System
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Jeanette Becker
Address
Veenpluis 4-6 Best Noord-Brabant NL 5684 pc 5684 pc

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code OWB  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K252735C-beamPulmera, Inc.2026-05-22
K252503Intelligent NRCanon, Inc.2026-04-30
K254173ARTIS icono floor; ARTIS icono biplane; ARTIS icono ceiling; ARTIS phenoSiemens Medical Solutions USA, Inc.2026-04-24
K253752ARTIS genio floor; ARTIS icono.explore floorSiemens Medical Solutions USA, Inc.2026-04-23
K252229BELLIGER ACEGenoray Co., Ltd.2026-04-02
K252099TriniasShimadzu Corporation2026-03-24
K253584Alphenix, INFX-8000V/B, INFX-8000V/S, V9.6 with aEvolve Imaging (FOV Extension)Canon Medical Systems Corporation2026-03-10
K252500CARA SystemCara Medical, Ltd.2026-02-20
K251992ArmSure Fluoroscopic Positioning SystemSavfe Co. , Ltd.2026-02-11
K254186Azurion R3.1Philips Medical Systems B.V.2026-01-16
K252068MC2 Portable X-ray SystemOxos Medical2025-12-22
K251893SKAN C PULSARSkanray Technologies Limited2025-12-16
K251199Allia MoveoGE Medical Systems SCS2025-12-09
K250241Cios SelectSiemens Medical Solutions USA, Inc.2025-11-04
K251827Azurion R3.1Philips Medical Systems B.V.2025-10-24

Legacy Summary#

summary

FDA Review#

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