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COLONIC SPLINTING OVERTUBE, MODEL 00711145

Page Type
Cleared 510(K)
510(k) Number
K092221
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2009
Days to Decision
90 days
Submission Type
Summary

COLONIC SPLINTING OVERTUBE, MODEL 00711145

Page Type
Cleared 510(K)
510(k) Number
K092221
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/20/2009
Days to Decision
90 days
Submission Type
Summary