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Veuron-Brain-mN1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K203279
510(k) Type
Traditional
Applicant
Heuron Co., Ltd.
Country
South Korea
FDA Decision
Substantially Equivalent
Decision Date
7/12/2022
Days to Decision
613 days
Submission Type
Summary