Bio-Feedback Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bio-Feedback Systems, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Bio-Feedback Systems, Inc. has 11 FDA 510(k) cleared neurology devices. Based in Mchenry, US.
Historical record: 11 cleared submissions from 1977 to 1991.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bio-Feedback Systems, Inc.
11 devices
Cleared
Apr 12, 1991
MINIATURE ELECTRODERMAL RESPONSE TRAINER EDR-002
Neurology
134d
Cleared
Apr 10, 1991
MINIATURE TEMPERATURE TRAINER MODEL DT-002
Neurology
132d
Cleared
Feb 16, 1990
MULTI-CHANNEL ISOLATION AMPLIFIER (MCIA)
Neurology
44d
Cleared
Jun 06, 1986
ISOLATED SOLID-STATE RELAY MULTIPLEXER & F/F CONV
Neurology
87d
Cleared
Sep 01, 1983
FEEDBACK EMG SYSTEM PE-020
Neurology
45d
Cleared
Oct 08, 1981
ISOLATED VOLTAGE/FREQUENCY CONVERTER
Neurology
23d
Cleared
Jan 09, 1980
FEEDBACK EDR SYSTEM MODEL ME-1
Neurology
14d
Cleared
Jun 24, 1977
ANALOG QUANTIFIER MODEL AQ-100
Neurology
16d
Cleared
May 10, 1977
FEEDBACK EDR SYSTEM MODEL EDR-100
Neurology
8d
Cleared
Apr 26, 1977
FEEDBACK EMG SYSTEM, MODEL PE-L00
Neurology
19d
Cleared
Feb 24, 1977
TEMPERATURE FEEDBACK SYS, MODEL DT100
Neurology
13d