FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MULTI-CHANNEL ISOLATION AMPLIFIER (MCIA)

K Number: K900063 · Decision Feb 16, 1990
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
52
Applicant Total
11
Review Days
44

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Basic Information

Device Name
MULTI-CHANNEL ISOLATION AMPLIFIER (MCIA)
K Number
K900063
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1835
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Bio-Feedback Systems, Inc.
Date Received
January 3, 1990
Decision Date
February 16, 1990
Product Code
GWL
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GWL Amplifier, Physiological Signal

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GWL), ordered by most recent decision date.

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Other Clearances by Bio-Feedback Systems, Inc.

K Number Device Name
K905372 MINIATURE ELECTRODERMAL RESPONSE TRAINER EDR-002
K905373 MINIATURE TEMPERATURE TRAINER MODEL DT-002
K860914 ISOLATED SOLID-STATE RELAY MULTIPLEXER & F/F CONV
K832333 FEEDBACK EMG SYSTEM PE-020
K812619 ISOLATED VOLTAGE/FREQUENCY CONVERTER
K792659 FEEDBACK EDR SYSTEM MODEL ME-1
K771023 ANALOG QUANTIFIER MODEL AQ-100
K770790 FEEDBACK EDR SYSTEM MODEL EDR-100
K770663 FEEDBACK EMG SYSTEM, MODEL PE-L00
K770270 TEMPERATURE FEEDBACK SYS, MODEL DT100
Search all 11 clearances from Bio-Feedback Systems, Inc. →