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FUJIFILM Double Balloon Endoscope EI580BT

Page Type
Cleared 510(K)
510(k) Number
K183032
510(k) Type
Traditional
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
6/24/2019
Days to Decision
235 days
Submission Type
Summary

FUJIFILM Double Balloon Endoscope EI580BT

Page Type
Cleared 510(K)
510(k) Number
K183032
510(k) Type
Traditional
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
6/24/2019
Days to Decision
235 days
Submission Type
Summary