Litton Medical Electronics - FDA 510(k) Cleared Devices
38
Total
38
Cleared
0
Denied
Litton Medical Electronics has 38 FDA 510(k) cleared cardiovascular devices. Based in Walker, US.
Historical record: 38 cleared submissions from 1982 to 1985.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Litton Medical Electronics
38 devices
Cleared
May 16, 1985
RECOMED BLOOD-FLOW METER H236-052-02
Cardiovascular
464d
Cleared
Nov 20, 1984
RECOMED CARDIAC OUTPUT METER 236067-
Cardiovascular
293d
Cleared
Nov 20, 1984
SERVOMED ARRHYCOMP CENTRAL MONITOR SYS
Cardiovascular
266d
Cleared
Oct 29, 1984
SERVOMED PULSE AMPLIFIER MODULE-206-
Cardiovascular
265d
Cleared
Oct 26, 1984
SERVOMED BASIC BEDSIDE UNIT SMV 110TP
Cardiovascular
262d
Cleared
Sep 20, 1984
SERVOMED MEDIVISION SCOPE SMV-235
Cardiovascular
245d
Cleared
Sep 20, 1984
SERVOMED OXCARDIORE SPIROGRAPH 324/111
Cardiovascular
209d
Cleared
Jun 01, 1984
SERVOMED BASIC BEDSIDE UNIT SMA 102-
Cardiovascular
326d
Cleared
Jun 01, 1984
2-CHANNEL RECORDER
Cardiovascular
288d
Cleared
Jun 01, 1984
I-CHANNEL RECORDER
Cardiovascular
288d
Cleared
Jun 01, 1984
RECOMB ECG PREAMPLIFIER/206 069 03
Cardiovascular
154d
Cleared
Jun 01, 1984
SERVOMED DIGITAL DISPLAY MODULE
Cardiovascular
115d
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