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

X10 HEADSET WITH X-SERIES BASIC SOFTWARE, X24 HEADSET WITH X-SERIES BASIC SOFTWARE

K Number: K131383 · Decision Nov 27, 2013
Classifications
1
FEI Numbers
96
Registration Numbers
96
Same Product Code
188
Applicant Total
14
Review Days
197

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Basic Information

Device Name
X10 HEADSET WITH X-SERIES BASIC SOFTWARE, X24 HEADSET WITH X-SERIES BASIC SOFTWARE
K Number
K131383
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1400
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Advanced Brain Monitoring, Inc.
Date Received
May 14, 2013
Decision Date
November 27, 2013
Product Code
GWQ
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
GWQ Full-Montage Standard Electroencephalograph

Similar 510(k) Clearances

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Other Clearances by Advanced Brain Monitoring, Inc.

K Number Device Name
K153412 Sleep Profiler
K152040 X8 System - Sleep Profiler (SP40), X8 System - Sleep Profiler PSG2 (SP29), X8 System - Stat X8 (XS29)
K140190 NIGHT SHIFT
K130007 SLEEP PROFILER
K130013 X4 SYSTEM
K120450 SLEEP PROFILER
K120447 X4
K112514 APNEA RISK EVALUATION SYSTEM (ARES)
K111110 APNEA GUARD
K111194 APNEA RISK EVALUATION SYSTEM (ARES)
Search all 14 clearances from Advanced Brain Monitoring, Inc. →