Schiller AG - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
FDA 510(k) cleared devices by Schiller AG Cardiovascular ✕
14 devices
Cleared
Jul 06, 2023
ARGUS PB-3000
Cardiovascular
451d
Cleared
Mar 02, 2020
CARDIOVIT AT-102 G2
Cardiovascular
447d
Cleared
Jul 19, 2017
CARDIOVIT FT-1
Cardiovascular
177d
Cleared
May 06, 2016
Diagnostic Station DS20
Cardiovascular
288d
Cleared
Nov 12, 2010
WELCH ALLYN 1500 PATIENT MONITOR
Cardiovascular
156d
Cleared
Mar 07, 2007
BP-200 PLUS
Cardiovascular
75d
Cleared
May 19, 2006
ARGUS, MODEL LCM
Cardiovascular
184d
Cleared
Aug 09, 2005
BR 102 PLUS BLOOD PRESSURE HOLTER SYSTEM
Cardiovascular
76d
Cleared
May 04, 2005
CARDIOVIT AT-10PLUS
Cardiovascular
49d
Cleared
Aug 24, 2004
MONITORING SYSTEM, MODEL ARGUS PB-2200
Cardiovascular
270d
Cleared
Apr 14, 2004
CARDIOVIT AT-102
Cardiovascular
331d
Cleared
Apr 08, 2002
MONITORING SYSTEM,MODEL ARGUS PB-1000
Cardiovascular
266d