FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AUTOBAND LIGATOR

K Number: K132535 · Decision Aug 23, 2013
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
14
Applicant Total
27
Review Days
10

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Basic Information

Device Name
AUTOBAND LIGATOR
K Number
K132535
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.4400
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Endochoice, Inc.
Date Received
August 13, 2013
Decision Date
August 23, 2013
Product Code
MND
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MND Ligator, Esophageal

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Other Clearances by Endochoice, Inc.

K Number Device Name
K160275 Fuse Endoscopic System with FuseBox Processor
K161482 EndoChoice Water Bottle Cap Irrigation System
K161167 Seal Single-Use Biopsy Valve
K160403 SmartStart Air/Water and Suction Valves
K153588 EndoChoice Water Bottle Cap System
K151475 EndoChoice Select Injection Needle
K152182 Fuse Gastroscopy System
K152580 rescuenet
K142155 ENDOCHOICE WATER BOTTLE CAP SYSTEM
K140472 BONASTENT TRACHEAL / BRONCHIAL
Search all 27 clearances from Endochoice, Inc. →