Schiller America, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Schiller America, Inc. has 10 FDA 510(k) cleared cardiovascular devices. Based in Tustin, US.
Historical record: 10 cleared submissions from 1990 to 1998.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
10 devices
Cleared
Aug 25, 1998
MICROVIT MT-100
Cardiovascular
329d
Cleared
Aug 25, 1998
MT-200
Cardiovascular
328d
Cleared
Jun 25, 1997
CARDIOVIT CS-200
Cardiovascular
107d
Cleared
Dec 19, 1995
CARDIOVIT AT-1C, AT-2C
Cardiovascular
152d
Cleared
Oct 27, 1995
MINISCOPE MS-3
Cardiovascular
58d
Cleared
May 19, 1995
CARDIOVIT AT-5C
Cardiovascular
421d
Cleared
Mar 16, 1995
CARDIOVIT AT-1, P-80
Cardiovascular
85d
Cleared
Nov 03, 1992
CARDIOVIT CS-100
Cardiovascular
364d
Cleared
Jan 09, 1990
SCHILLER MODEL SP-100 SPIROVIT(TM)
Anesthesiology
77d
Cleared
Jan 09, 1990
SCHILLER MODEL SP-200 SPIROVIT(TM)
Anesthesiology
77d