ClearanceBrief
Company ยท GB

Deltex Medical Limited

FDA 510(k) clearances and medical device recalls filed under this name, 1995 to 2018. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DPWFlowmeter, Blood, Cardiovascular6
DPTProbe, Blood-Flow, Extravascular3

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 28, 2018K172457Deltex Medical CardioQ-EDM+, Deltex Medical CardioQ-EDM
Deltex Medical Limited, GB
DPW
Jul 24, 2015K150347Deltex Medical CardioQ-EDM, Deltex Medical CardioQ-EDM+
Deltex Medical Limited, GB
DPW
Jan 22, 2015K142932Deltex Medical KDP72 Doppler Probe
Deltex Medical Limited, GB
DPT
Oct 10, 2013K132139DELTEX MEDICAL CARDIOQ-EDM+
Deltex Medical Limited
DPW
Oct 20, 2011K111542DELTEX MEDICAL CARDIOQ EDM
Deltex Medical Limited, GB
DPW
Jan 29, 2009K073593I2S DOPPLER PROBE ( 6 HOUR), I2S DOPPLER PROBE (24 HOUR), I2C DOPPLER PROBE (72 HOUR), MODELS 9090-7015, 9090-7016
Deltex Medical Limited, GB
DPT
Mar 8, 2006K052989DP240 240 HOUR DOPPLER PROBE
Deltex Medical, GB
DPT
Aug 6, 2003K031706CARDIOQ, MODEL 9051-7005
Deltex Medical, GB
DPW
Nov 7, 1995K951369EDM
Deltex Medical
DPW

Latest recalls

DateFirm and productCodeLinked 510(k)
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