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FUJIFILM Surgical System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162836
510(k) Type
Traditional
Applicant
FUJIFILM New Development U.S.A., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/2017
Days to Decision
153 days
Submission Type
Summary