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FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EB-530US

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121035
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2012
Days to Decision
60 days
Submission Type
Summary

FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EB-530US

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K121035
510(k) Type
Traditional
Applicant
FUJIFILM MEDICAL SYSTEM U.S.A., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2012
Days to Decision
60 days
Submission Type
Summary