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
Cleared
May 09, 1984
FUKUDA DENSHI FX-102 AUTO-SINGLE CHAN
Cardiovascular
210d
Cleared
Mar 13, 1984
FCP-11ECG
Cardiovascular
Cleared
Jul 28, 1983
AMBULATORY ECG EVENT RECORDER
Cardiovascular
129d
Cleared
Apr 06, 1983
COMPUTER-AIDED ELECTROCARDIOGRAPH FCP-13
Cardiovascular
121d
Cleared
Apr 06, 1983
COMPUTER-AIDED ELECTROCARDIOGRAPH FCP200
Cardiovascular
121d
Cleared
Dec 30, 1982
FUKUDA DENSHI 6-CHANNEL AUTO. ELECTRO-
Cardiovascular
24d
Cleared
Dec 14, 1981
FUKUDA DENSHI...ELECTROCARDIOGRAPH FD-36
Cardiovascular
48d
Cleared
Dec 02, 1981
FUKUDA DENSHI CARDIMAX FK-12
Cardiovascular
36d
Cleared
Dec 02, 1981
FUKUDA DENSHI CARDIMAX FK-11
Cardiovascular
36d