Brentwood Instruments, Inc. - FDA 510(k) Cleared Devices
21
Total
20
Cleared
0
Denied
Brentwood Instruments, Inc. has 20 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 20 cleared submissions from 1981 to 1990.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
21 devices
Cleared
Mar 01, 1990
SPIROSCAN 4000
Anesthesiology
79d
Cleared
Aug 02, 1988
RHYTHMSCAN HR HOLTER RECORDER
Cardiovascular
55d
Cleared
Feb 22, 1988
RHYTHMSCAN
Cardiovascular
306d
Cleared
Mar 31, 1986
FUKUDA DENSHI CARDIMAX FCP-211
Cardiovascular
87d
Cleared
Feb 06, 1986
CARDIMAX FX-1164
Cardiovascular
133d
Cleared
Feb 04, 1986
CARDIMAX FX-406U
Cardiovascular
84d
Cleared
Jul 01, 1985
SPIRO SCAN
Anesthesiology
102d
Cleared
May 15, 1985
R-1000 ECG RECEIVER
Cardiovascular
57d
Cleared
May 15, 1985
T-1000 ECG TRANSMITTER
Cardiovascular
57d
Cleared
Mar 01, 1985
BRENTWOOD EZ SCAN 200 AMBULATORY ECG
Cardiovascular
214d
Cleared
Jan 10, 1985
FUKUDA DENSHI MODEL FCP-220
Cardiovascular
52d
Cleared
Sep 11, 1984
FUKUDA DENSHI FX-302 AUTO/THREE CHAN
Cardiovascular
335d