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R-40 EEG Amplifier

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151600
510(k) Type
Traditional
Applicant
LIFELINES LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/23/2015
Days to Decision
133 days
Submission Type
Summary

R-40 EEG Amplifier

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K151600
510(k) Type
Traditional
Applicant
LIFELINES LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
10/23/2015
Days to Decision
133 days
Submission Type
Summary