Last synced on 25 November 2022 at 11:04 pm

FUJINON G5 DUODENSCOPES; G5 DUODENOSCOPES, ED-450XT5, ED-250XT5

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042076
510(k) Type
Traditional
Applicant
FUJINON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2004
Days to Decision
108 days
Submission Type
Summary

FUJINON G5 DUODENSCOPES; G5 DUODENOSCOPES, ED-450XT5, ED-250XT5

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K042076
510(k) Type
Traditional
Applicant
FUJINON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2004
Days to Decision
108 days
Submission Type
Summary