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FUJIFILM Ultrasonic Endoscope

Page Type
Cleared 510(K)
510(k) Number
K181763
510(k) Type
Special
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/27/2018
Days to Decision
24 days
Submission Type
Summary

FUJIFILM Ultrasonic Endoscope

Page Type
Cleared 510(K)
510(k) Number
K181763
510(k) Type
Special
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
7/27/2018
Days to Decision
24 days
Submission Type
Summary