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

AmplifEYE

K Number: K160846 · Decision Jul 14, 2016
Classifications
1
FEI Numbers
116
Registration Numbers
116
Same Product Code
100
Applicant Total
11
Review Days
108

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Basic Information

Device Name
AmplifEYE
K Number
K160846
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.1500
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medivators, Inc.
Date Received
March 28, 2016
Decision Date
July 14, 2016
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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