FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

BONASTENT TRACHEAL / BRONCHIAL

K Number: K140472 · Decision Oct 17, 2014
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
44
Applicant Total
27
Review Days
234

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Basic Information

Device Name
BONASTENT TRACHEAL / BRONCHIAL
K Number
K140472
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3720
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Endochoice, Inc.
Date Received
February 25, 2014
Decision Date
October 17, 2014
Product Code
JCT
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
JCT Prosthesis, Tracheal, Expandable

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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
K141598 FUSE COLONOSCOPY SYSTEM
Search all 27 clearances from Endochoice, Inc. →