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8-CH Electroencephalography Amplifier

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201747
510(k) Type
Traditional
Applicant
Hipposcreen Neurotech Corp.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
12/27/2020
Days to Decision
184 days
Submission Type
Summary

8-CH Electroencephalography Amplifier

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K201747
510(k) Type
Traditional
Applicant
Hipposcreen Neurotech Corp.
Country
Taiwan
FDA Decision
Substantially Equivalent
Decision Date
12/27/2020
Days to Decision
184 days
Submission Type
Summary