FDA 510(k) FDA class 2 Unknown 🇨🇦 Canada

BONASTENT BILIARY

K Number: K140760 · Decision Jun 16, 2014
Classifications
1
FEI Numbers
143
Registration Numbers
143
Same Product Code
473
Applicant Total
27
Review Days
82

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Basic Information

Device Name
BONASTENT BILIARY
K Number
K140760
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5010
Medical Specialty
Gastroenterology, Urology
Decision
Unknown
Statement or Summary
Summary
Applicant
Endochoice, Inc.
Date Received
March 26, 2014
Decision Date
June 16, 2014
Product Code
FGE
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
FGE Stents, Drains And Dilators For The Biliary Ducts

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FGE), ordered by most recent decision date.

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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. →