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FUJIFILM Video Laparoscope

Page Type
Cleared 510(K)
510(k) Number
K202130
510(k) Type
Special
Applicant
Fujifilm Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/20/2020
Days to Decision
20 days
Submission Type
Summary

FUJIFILM Video Laparoscope

Page Type
Cleared 510(K)
510(k) Number
K202130
510(k) Type
Special
Applicant
Fujifilm Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
8/20/2020
Days to Decision
20 days
Submission Type
Summary