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Visera Elite II Video System Center, Visera Elite II Endoeye 3D

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K193026
510(k) Type
Traditional
Applicant
Olympus Medical Systems Corp.
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
4/3/2020
Days to Decision
156 days
Submission Type
Summary