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Neoscope 3D - 3D Digital Video Endoscopic System (Rigid/Flexible)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152619
510(k) Type
Traditional
Applicant
PROSURG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/2016
Days to Decision
228 days
Submission Type
Summary