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Video Laparoscope, Video Processor, Light Source

Page Type
Cleared 510(K)
510(k) Number
K192918
510(k) Type
Traditional
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
2/20/2020
Days to Decision
128 days
Submission Type
Summary

Video Laparoscope, Video Processor, Light Source

Page Type
Cleared 510(K)
510(k) Number
K192918
510(k) Type
Traditional
Applicant
FUJIFILM Corporation
Country
Japan
FDA Decision
Substantially Equivalent
Decision Date
2/20/2020
Days to Decision
128 days
Submission Type
Summary