American Telecare, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Telecare, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
American Telecare, Inc. has 9 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Historical record: 9 cleared submissions from 1995 to 2003. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by American Telecare, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Telecare, Inc.
9 devices
Cleared
Aug 19, 2003
NX SYSTEM
Cardiovascular
209d
Cleared
Jun 28, 2001
AVIVA SYSTEM, MODEL SL 2020
Cardiovascular
184d
Cleared
Jan 13, 2000
AVIVA SYSTEM, MODEL SL1010
Cardiovascular
85d
Cleared
Jul 15, 1998
AVIVA SYSTEMS MODEL NUMBERS 1010, 2020
Cardiovascular
77d
Cleared
Dec 29, 1997
DIGITAL PERSONAL TELEMEDICINE MODULE, DIGITAL PTM 1
Cardiovascular
80d
Cleared
Feb 24, 1997
CARETONE II
Cardiovascular
164d
Cleared
Dec 17, 1996
PERSONAL TELEMEDICINE MODULE
Cardiovascular
34d
Cleared
Sep 09, 1996
PERSONAL TELEMEDICINE SYSTEM
Cardiovascular
444d
Cleared
May 17, 1995
TELPHONIC STETHOSCOPE
Cardiovascular
182d