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

APNEA RISK EVALUATION SYSTEM (ARES)

K Number: K110705 · Decision Apr 14, 2011
Classifications
1
FEI Numbers
84
Registration Numbers
84
Same Product Code
160
Applicant Total
14
Review Days
31

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Basic Information

Device Name
APNEA RISK EVALUATION SYSTEM (ARES)
K Number
K110705
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
868.2375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Advanced Brain Monitoring, Inc.
Date Received
March 14, 2011
Decision Date
April 14, 2011
Product Code
MNR
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
MNR Ventilatory Effort Recorder

Similar 510(k) Clearances

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

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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
K131383 X10 HEADSET WITH X-SERIES BASIC SOFTWARE, X24 HEADSET WITH X-SERIES BASIC SOFTWARE
K130007 SLEEP PROFILER
K130013 X4 SYSTEM
K120450 SLEEP PROFILER
K120447 X4
K112514 APNEA RISK EVALUATION SYSTEM (ARES)
K111110 APNEA GUARD
Search all 14 clearances from Advanced Brain Monitoring, Inc. →