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ENDOSEE MODEL 8000 U-SCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123151
510(k) Type
Traditional
Applicant
ENDOSEE CORP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2013
Days to Decision
150 days
Submission Type
Summary

ENDOSEE MODEL 8000 U-SCOPE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123151
510(k) Type
Traditional
Applicant
ENDOSEE CORP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2013
Days to Decision
150 days
Submission Type
Summary