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

ENDOSCOPIC INTRODUCER

K Number: K123013 · Decision Mar 22, 2013
Classifications
1
FEI Numbers
116
Registration Numbers
116
Same Product Code
100
Applicant Total
15
Review Days
175

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Basic Information

Device Name
ENDOSCOPIC INTRODUCER
K Number
K123013
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Novadaq Technologies, Inc.
Date Received
September 28, 2012
Decision Date
March 22, 2013
Product Code
FED
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
FED Endoscopic Access Overtube, Gastroenterology-Urology

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