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AUTOBAND LIGATOR

Page Type
Cleared 510(K)
510(k) Number
K132535
510(k) Type
Special
Applicant
Endochoice, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2013
Days to Decision
10 days
Submission Type
Summary

AUTOBAND LIGATOR

Page Type
Cleared 510(K)
510(k) Number
K132535
510(k) Type
Special
Applicant
Endochoice, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2013
Days to Decision
10 days
Submission Type
Summary