ClearanceBrief
Company ยท US

Litton Medical Systems

FDA 510(k) clearances and medical device recalls filed under this name, 1976 to 1977. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
IZOGenerator, High-Voltage, X-Ray, Diagnostic3
JAASystem, X-Ray, Fluoroscopic, Image-Intensified2
ITYAssembly, Tube Housing, X-Ray, Diagnostic1
IXRTable, Radiographic, Tilting1
KPWDevice, Beam Limiting, X-Ray, Diagnostic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 1, 1977K770338X-RAY CONTROL & X-RAY HV GENERATOR
Litton Medical Systems
IZO
Mar 1, 1977K770337FLUOROSCOPIC ASSEMBLY, IMAGE INTENS.
Litton Medical Systems
JAA
Mar 1, 1977K770336X-RAY TUBE, ROTATING ANODE
Litton Medical Systems
ITY
Mar 1, 1977K770334TILTING X-RAY TABLE
Litton Medical Systems
IXR
Mar 1, 1977K770333FLUOROSCOPE, C-ARM
Litton Medical Systems
JAA
Feb 28, 1977K770335COLLIMATOR, AUTOMATIC
Litton Medical Systems
KPW
Sep 15, 1976K760569THREE PHASE X-RAY CONTROLS & HV GENERATORS
Litton Medical Systems
IZO
Sep 15, 1976K760568SINGLE PHASE X-RAY CONTROLS & HV GENERATORS
Litton Medical Systems
IZO

Latest recalls

DateFirm and productCodeLinked 510(k)
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