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ANAL RECTAL OVERTUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131598
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2014
Days to Decision
268 days
Submission Type
Statement

ANAL RECTAL OVERTUBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K131598
510(k) Type
Traditional
Applicant
UNITED STATES ENDOSCOPY GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/2014
Days to Decision
268 days
Submission Type
Statement