ClearanceBrief
Company ยท US

Datex Medical Instrumentation, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1991 to 1997. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
CBSAnalyzer, Gas, Halothane, Gaseous-Phase (Anesthetic Conc.)1
CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-Phase1
DQKComputer, Diagnostic, Programmable1
DXNSystem, Measurement, Blood-Pressure, Non-Invasive1
KOIStimulator, Nerve, Peripheral, Electric1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 28, 1997K955026AS/3 NMT MODULE
Datex Medical Instrumentation, Inc.
KOI
May 31, 1996K961063AS/3 CARDIAC OUTPUT & SVO2 MODULE
Datex Medical Instrumentation, Inc.
DQK
May 3, 1996K960490AS/3 COMPACT AIRWAY MODULE M-CAIOV
Datex Medical Instrumentation, Inc.
CBS
Sep 27, 1995K953006AS/3 NETWORK LINK
Datex Medical Instrumentation, Inc.
CCK
Sep 5, 1991K912530CARDIOCAP II(TM)
Datex Medical Instrumentation, Inc.
DXN

Latest recalls

DateFirm and productCodeLinked 510(k)
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