Medical Device Manufacturer · CH , Baar

Schiller AG - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1985
16
Total
16
Cleared
0
Denied

Schiller AG has 16 FDA 510(k) cleared cardiovascular devices. Based in Baar, CH.

Latest FDA clearance: Jul 2023. Active since 1985.

Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.

16 devices
1–12 of 16
ARGUS PB-3000
K221056 · MHX Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) · Cardiovascular
Jul 2023 451d
CARDIOVIT AT-102 G2
K183425 · DPS Electrocardiograph · Cardiovascular
Mar 2020 447d
CARDIOVIT FT-1
K170182 · DPS Electrocardiograph · Cardiovascular
Jul 2017 177d
Diagnostic Station DS20
K152043 · DPS Electrocardiograph · Cardiovascular
May 2016 288d
WELCH ALLYN 1500 PATIENT MONITOR
K101619 · MHX Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) · Cardiovascular
Nov 2010 156d
BP-200 PLUS
K063814 · DXN System, Measurement, Blood-pressure, Non-invasive · Cardiovascular
Mar 2007 75d
ARGUS, MODEL LCM
K053207 · MHX Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) · Cardiovascular
May 2006 184d
BR 102 PLUS BLOOD PRESSURE HOLTER SYSTEM
K051368 · DXN System, Measurement, Blood-pressure, Non-invasive · Cardiovascular
Aug 2005 76d
CARDIOVIT AT-10PLUS
K050686 · DPS Electrocardiograph · Cardiovascular
May 2005 49d
MONITORING SYSTEM, MODEL ARGUS PB-2200
K033738 · DSK Computer, Blood-pressure · Cardiovascular
Aug 2004 270d
CARDIOVIT AT-102
K031557 · DPS Electrocardiograph · Cardiovascular
Apr 2004 331d
MONITORING SYSTEM,MODEL ARGUS PB-1000
K012226 · MHX Monitor, Physiological, Patient(with Arrhythmia Detection Or Alarms) · Cardiovascular
Apr 2002 266d
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