510(k) K132535

AUTOBAND LIGATOR by Endochoice, Inc. — Product Code MND

K132535 is an FDA 510(k) premarket notification submitted by Endochoice, Inc. for the device "AUTOBAND LIGATOR". The FDA issued a decision of Substantially Equivalent on August 23, 2013. The device falls under product code MND (Ligator, Esophageal), a Class II device regulated under 21 CFR 876.4400. Endochoice, Inc. has at least 10 other 510(k) clearances on record.

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