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PENTAX Medical VIVIDEO ENT Videoscope Solution

Page Type
Cleared 510(K)
510(k) Number
K171011
510(k) Type
Traditional
Applicant
Pentax Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2018
Days to Decision
470 days
Submission Type
Summary

PENTAX Medical VIVIDEO ENT Videoscope Solution

Page Type
Cleared 510(K)
510(k) Number
K171011
510(k) Type
Traditional
Applicant
Pentax Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/2018
Days to Decision
470 days
Submission Type
Summary