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

PSA4000 EEG MONITOR WITH FRONTAL PSI

K Number: K020671 · Decision Oct 4, 2002
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
37
Applicant Total
22
Review Days
217

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Basic Information

Device Name
PSA4000 EEG MONITOR WITH FRONTAL PSI
K Number
K020671
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Physiometrix, Inc.
Date Received
March 1, 2002
Decision Date
October 4, 2002
Product Code
OLW
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
OLW Index-Generating Electroencephalograph Software

Similar 510(k) Clearances

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

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Other Clearances by Physiometrix, Inc.

K Number Device Name
K051874 SEDLINE SEDATION MONITOR WITH FRONTAL PSI AND SEDTRACE EEG ELECTROSE SET
K033999 SEDLINE WITH FRONTAL PSI
K020670 MODEL 4310 PSARRAY2 EEG ELECTRODE
K001069 MODEL 4000 EEG MONITOR WITH PSI (PSA4000)
K001055 MODEL 4300 PSARRAY EEG ELECTRODE SET
K970942 MODEL 1320, NEUROLINK II NEUROMONITORING SYSTEM
K970694 MODEL 1700, HYDRO PREP
K962447 EQUINOX DIGITAL EEG SYSTEM
K962157 MODEL 1310 NEUROLINK NEUROMONITORING SYSTEM
K961609 MODEL 1220, OR E-NET (54-62 CM)
Search all 22 clearances from Physiometrix, Inc. →