FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

TRACTION POLYPECTOMY SNARE

K Number: K140923 · Decision Nov 18, 2014
Classifications
1
FEI Numbers
63
Registration Numbers
63
Same Product Code
62
Applicant Total
14
Review Days
222

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Basic Information

Device Name
TRACTION POLYPECTOMY SNARE
K Number
K140923
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.4300
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Ovesco Endoscopy AG
Date Received
April 10, 2014
Decision Date
November 18, 2014
Product Code
FDI
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
FDI Snare, Flexible

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K221385 LiftUp (Ref. Nr.: 200.56.01), LiftUp Kit (Ref. Nr.: 200.56.02)
K200684 gastroduodenal FTRD Set
K183309 stentfix OTSC System Set
DEN160014 remOVE System
K170867 FTRD System Set
K153550 FTRD System Set
K150067 OTSC Proctology
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