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BrainScope TBI

Page Type
Cleared 510(K)
510(k) Number
K190815
510(k) Type
Traditional
Applicant
Brainscope Company, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2019
Days to Decision
166 days
Submission Type
Summary

BrainScope TBI

Page Type
Cleared 510(K)
510(k) Number
K190815
510(k) Type
Traditional
Applicant
Brainscope Company, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2019
Days to Decision
166 days
Submission Type
Summary