Schiller AG - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Schiller AG has 16 FDA 510(k) cleared cardiovascular devices. Based in Baar, CH.
Last cleared in 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
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
Cleared
May 12, 2000
SPIROVIT SP-2, PNEUMOCHECK II
Anesthesiology
263d
Cleared
Apr 30, 1999
SPIROVIT, MODEL SP-250
Anesthesiology
169d
Cleared
Apr 25, 1985
CARDIOVIT CS-6 ECG-RECORDER
Cardiovascular
63d
Cleared
Jan 24, 1985
CARDIOVIT CV-3
Cardiovascular
304d