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Litton Medical Systems

FDA Regulatory Profile

Litton Medical Systems has 0 FDA recalls, 0 inspections, 8 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Mar 1, 1977

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances8Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K770333FLUOROSCOPE, C-ARMMar 1, 1977
K770334TILTING X-RAY TABLEMar 1, 1977
K770336X-RAY TUBE, ROTATING ANODEMar 1, 1977
K770337FLUOROSCOPIC ASSEMBLY, IMAGE INTENS.Mar 1, 1977
K770338X-RAY CONTROL & X-RAY HV GENERATORMar 1, 1977
K770335COLLIMATOR, AUTOMATICFeb 28, 1977
K760568SINGLE PHASE X-RAY CONTROLS & HV GENERATORSSep 15, 1976
K760569THREE PHASE X-RAY CONTROLS & HV GENERATORSSep 15, 1976

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.