ClearanceBrief
Company ยท US

Ld Technology, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2009 to 2020. Name variants (Inc, Corp, punctuation) are merged.

14510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MWIMonitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)4
DXNSystem, Measurement, Blood-Pressure, Non-Invasive3
GZODevice, Galvanic Skin Response Measurement3
JOMPlethysmograph, Photoelectric, Pneumatic Or Hydraulic2
DQAOximeter1
MNWAnalyzer, Body Composition1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
May 15, 2020K200287BP-BT Kiosk
Ld Technology, LLC
DXN
Apr 27, 2020K200141Oxi-W System
Ld Technology, LLC
MWI
Dec 19, 2017K173696TBL-ABI System
Ld Technology, LLC
JOM
Jul 6, 2016K160956LD-Oxi system
Ld Technology, LLC
MWI
Sep 24, 2015K152216SudoC
Ld Technology, LLC
GZO
Jul 22, 2015K143152TM-ABI system
Ld Technology, LLC
JOM
May 22, 2014K140412ANS1 SOFTWARE
Ld Technology, LLC
DXN
Jun 28, 2013K131568SUDO PATH
Ld Technology, LLC
GZO
Apr 11, 2013K130056PATIENT MONITOR
Ld Technology, LLC
MWI
Mar 2, 2012K113264ELECTRO SENSOR COMPLEX SOFTWARE (ES COMPLEX SOFTWARE)
Ld Technology, LLC
DXN
Mar 29, 2011K103026ELECTRO SENSOR -BODY COMPOSITION
Ld Technology, LLC
MNW
Dec 10, 2010K102166ELECTRO INTERSTITIAL SCAN
Ld Technology, LLC
GZO
Sep 10, 2010K102442E.S.O. (ELECTRO SENSOR OXI)
Ld Technology, LLC
DQA
Feb 23, 2009K083229E.S TECK ( ELECTRO SENSOR TECK)
Ld Technology, LLC
MWI

Latest recalls

DateFirm and productCodeLinked 510(k)
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