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Neurescue device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210358
510(k) Type
Traditional
Applicant
Neurescue Aps
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
5/21/2021
Days to Decision
102 days
Submission Type
Summary

Neurescue device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K210358
510(k) Type
Traditional
Applicant
Neurescue Aps
Country
Denmark
FDA Decision
Substantially Equivalent
Decision Date
5/21/2021
Days to Decision
102 days
Submission Type
Summary