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FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EG-530UR2 AND EG-530UT2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120446
510(k) Type
Traditional
Applicant
FUJINON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2012
Days to Decision
181 days
Submission Type
Summary

FUJINON/FUJIFILM ULTRASONIC ENDOSCOPE EG-530UR2 AND EG-530UT2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K120446
510(k) Type
Traditional
Applicant
FUJINON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/2012
Days to Decision
181 days
Submission Type
Summary