FDA.reportPublic FDA data

510(k) K810274

Device
Clinix-r Tomographic Device
Applicant
PHILIPS MEDICAL SYSTEMS(CLEVELAND), INC.
510(k) number
K810274
Product code
IZF
Decision
Substantially Equivalent (SESE)
Decision date
1981-03-11
Date received
1981-02-02
Regulation
892.1740
Classification name
System, X-Ray, Tomographic
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code IZF#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K252649TAP2DNano-X Imaging , Ltd.2026-02-02
K252133Adaptix Ortho350Adaptix Limited2025-11-06
K250850Nanox.ARC XNano-X Imaging , Ltd.2025-04-16
K242395Nanox.ARCNano-X Imaging , Ltd.2024-12-04
K222934Nanox.ARCNano-X Imaging , Ltd.2023-04-28
K221949Ortho Device, ADAPTIX 3D Orthopedic Imaging SystemPausch Medical GmbH2023-01-26
K213081CLISIS SYSTEMS, Discovery RF180General Medical Merate S.P.A2021-10-26
K193262DR 600 with TomosynthesisAgfa N.V.2020-03-09
K183275DR 800 with TomosynthesisAgfa N.V.2019-02-01
K132261DISCOVERY XR656 WITH VOLUMERAD (DIGITAL TOMOSYNTHESIS)Ge Medical Systems, LLC2013-11-18
K121499FUJIFILM TOMOSYNTHESIS OPTION FOR FDR ACSELERATE STATIONARY X-RAY SYSTEMFujifilm Medical System U.S.A., Inc.2012-11-20
K013620MEDSTONE, UROPRO 2000, TOMOGRAPHIC OPTIONMedstone Intl., Inc.2002-01-22
K011290PROGNOST ES, MODEL 0302 0000Xmar Corp.2001-05-30
K973864COMBI ELEVATOR-2 & COMBI ELEVATOR-2 TOMOPausch Corp.1998-06-17
K973834CS2000 & CS2000 TOMOPausch Corp.1998-04-30