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FUJIFILM ENDOSCOPIC CO2 REGULATOR

Page Type
Cleared 510(K)
510(k) Number
K133976
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2014
Days to Decision
257 days
Submission Type
Summary

FUJIFILM ENDOSCOPIC CO2 REGULATOR

Page Type
Cleared 510(K)
510(k) Number
K133976
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2014
Days to Decision
257 days
Submission Type
Summary