Last synced on 14 November 2025 at 11:06 pm

ENTEROSCOPY OVERTUBE, MODEL 00712140

Page Type
Cleared 510(K)
510(k) Number
K100081
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2010
Days to Decision
90 days
Submission Type
Summary

ENTEROSCOPY OVERTUBE, MODEL 00712140

Page Type
Cleared 510(K)
510(k) Number
K100081
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/12/2010
Days to Decision
90 days
Submission Type
Summary