Brentwood Medical Technology Corp. is one of 20379 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Brentwood Medical Technology Corp. - FDA 510(k) Cleared Devices
Recent clearances: MIDMARK IQECG, IQVITALS AND IQVITALS SYSTEM, IQMARK EZ STRESS
7
Total
7
Cleared
0
Denied
Brentwood Medical Technology Corp. has 7 FDA 510(k) cleared medical devices. Based in Torrance, US.
Historical record: 7 cleared submissions from 2000 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Brentwood Medical Technology Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Brentwood Medical Technology Corp.
7 devices
Cleared
Mar 22, 2011
MIDMARK IQECG
Cardiovascular
99d
Cleared
May 26, 2010
IQVITALS AND IQVITALS SYSTEM
Cardiovascular
55d
Cleared
Mar 28, 2006
IQMARK EZ STRESS
Cardiovascular
165d
Cleared
Jun 11, 2003
IQMARK DIGITAL HOLTER
Cardiovascular
34d
Cleared
Feb 06, 2002
BRENTWOOD REAL TIME ST AND ARRHYTHMIA ANALYSIS SOFTWARE LIBRARY
Cardiovascular
90d
Cleared
Mar 09, 2001
TELEMED 12 LEAD RESTING ECG ANALYSIS LIBRARY
Cardiovascular
16d
Cleared
Nov 08, 2000
BRENTWOOD IQMARK DIGITAL SPIROMETER (INCLUDES DISPOSABLE PNEUMOTACH...
Anesthesiology
86d