Last synced on 14 November 2025 at 11:06 pm

ANAL RECTAL OVERTUBE

Page Type
Cleared 510(K)
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)
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