Litton Medical Electronics

FDA Regulatory Profile

Litton Medical Electronics has 0 FDA recalls, 0 inspections, 38 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
May 16, 1985

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances38Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K840522RECOMED BLOOD-FLOW METER H236-052-02May 16, 1985
K840439RECOMED CARDIAC OUTPUT METER 236067-Nov 20, 1984
K840899SERVOMED ARRHYCOMP CENTRAL MONITOR SYSNov 20, 1984
K840523SERVOMED PULSE AMPLIFIER MODULE-206-Oct 29, 1984
K840524SERVOMED BASIC BEDSIDE UNIT SMV 110TPOct 26, 1984
K840832SERVOMED OXCARDIORE SPIROGRAPH 324/111Sep 20, 1984
K840209SERVOMED MEDIVISION SCOPE SMV-235Sep 20, 1984
K8329982-CHANNEL RECORDERJun 1, 1984
K834600RECOMB ECG PREAMPLIFIER/206 069 03Jun 1, 1984
K833000I-CHANNEL RECORDERJun 1, 1984
K832250SERVOMED BASIC BEDSIDE UNIT SMA 102-Jun 1, 1984
K840521SERVOMED DIGITAL DISPLAY MODULEJun 1, 1984
K840525SERVOMED COMPACT MONITOR SMK 155-1/101Jun 1, 1984
K832095SEVOMED COMPACT MONITOR SMK 154-Mar 22, 1984
K832025SERVOMED COMPACT MONITOR SMK 155-7/101Mar 22, 1984
K832999RESPIRATION MONITORFeb 13, 1984
K832652OXY MONITOR 5-RANGE DUAL-THERMISTORDec 22, 1983
K832035SERVOMED COMPACT MONITOR SMK 155-9Nov 16, 1983
K832131SERVOMED CENTRAL STATION SMV 206Nov 16, 1983
K832022SERVOMED SMC 108/111-426-24, 111-426Nov 16, 1983