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FUJIFILM Duodenoscope Model

Page Type
Cleared 510(K)
510(k) Number
K181745
510(k) Type
Traditional
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
3/28/2019
Days to Decision
269 days
Submission Type
Summary

FUJIFILM Duodenoscope Model

Page Type
Cleared 510(K)
510(k) Number
K181745
510(k) Type
Traditional
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
3/28/2019
Days to Decision
269 days
Submission Type
Summary