510(k) K132535

AUTOBAND LIGATOR by Endochoice, Inc. — Product Code MND

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 23, 2013
Date Received
August 13, 2013
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Ligator, Esophageal
Device Class
Class II
Regulation Number
876.4400
Review Panel
GU
Submission Type