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VISERA CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE V2, VISERA CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE VA2, VISERA CYSTO-NE

Page Type
Cleared 510(K)
510(k) Number
K133538
510(k) Type
Traditional
Applicant
Olympus Corporation OF The Americas
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2014
Days to Decision
262 days
Submission Type
Summary

VISERA CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE V2, VISERA CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE VA2, VISERA CYSTO-NE

Page Type
Cleared 510(K)
510(k) Number
K133538
510(k) Type
Traditional
Applicant
Olympus Corporation OF The Americas
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/7/2014
Days to Decision
262 days
Submission Type
Summary