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EG-530CT, EG-530D, EC-530DL, and ES-530WE Endoscopes

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142629
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2015
Days to Decision
240 days
Submission Type
Summary

EG-530CT, EG-530D, EC-530DL, and ES-530WE Endoscopes

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K142629
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2015
Days to Decision
240 days
Submission Type
Summary