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FUJIFILM Duodenoscope Model

Page Type
Cleared 510(K)
510(k) Number
K182051
510(k) Type
Special
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/2/2018
Days to Decision
63 days
Submission Type
Summary

FUJIFILM Duodenoscope Model

Page Type
Cleared 510(K)
510(k) Number
K182051
510(k) Type
Special
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
10/2/2018
Days to Decision
63 days
Submission Type
Summary