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APNEA RISK EVALUATION SYSTEM (ARES), MODEL 600

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071230
510(k) Type
Special
Applicant
Advanced Brain Monitoring, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2007
Days to Decision
153 days
Submission Type
Summary

APNEA RISK EVALUATION SYSTEM (ARES), MODEL 600

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071230
510(k) Type
Special
Applicant
Advanced Brain Monitoring, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2007
Days to Decision
153 days
Submission Type
Summary