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510(k) K770335

Device
COLLIMATOR, AUTOMATIC
Applicant
Litton Medical Systems
510(k) number
K770335
Product code
KPW
Decision
Substantially Equivalent (SESE)
Decision date
1977-02-28
Date received
1977-02-18
Regulation
892.1610
Classification name
Device, Beam Limiting, X-Ray, Diagnostic
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Third party reviewed
N

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 KPW#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K093596LUMOS, MODEL R 72BLumos, Inc.2010-01-12
K062788COLLIMATOR, MODEL M-38Umi International2006-12-28
K030487R 72Ralco S.R.L.2003-08-01
K954310BLA-800AToshiba Medical Systems1995-10-18
K946320R 302Ralco S.R.L.1995-05-11
K914184P2020-8-0 BEAM-LIMITING DEVICEPrecise Optics1991-11-27
K904587DENSICOMP 250L. Keroack Co.1991-01-24
K904044TF-63SAToshiba America Medical Systems, In.C1990-11-29
K904489EUREKA EXTENSION CYLINDERSEureka X-Ray Tube Corp.1990-10-15
K820306RALCO COLLIMATOR, AUTOMATIC RADIOGRAPHICTecnomed, Inc.1982-03-05
K820305RALCO COLLIMATORS, MANUAL RADIOGRAPHICTecnomed, Inc.1982-03-04
K820119PODIOSCOPE BY ARROWArrow X-Ray Corp.1982-02-18
K811450ALUMINUM FILTRATION SYSTEMWedge Filtration System1981-07-02
K791504AUTOMATIC POSITIVE BEAM COLLIMATORDial-X Instruments, Inc.1979-09-07
K781984COLLIMATOR, HEART CONTOURSiemens Corp.1978-12-04