FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

ApolloVue S100 Image System

K Number: K201552 · Decision Sep 2, 2020
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
45
Applicant Total
1
Review Days
84

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Basic Information

Device Name
ApolloVue S100 Image System
K Number
K201552
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Apollo Medical Optics, Ltd.
Date Received
June 10, 2020
Decision Date
September 2, 2020
Product Code
NQQ
Advisory Committee
Radiology
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
NQQ System, Imaging, Optical Coherence Tomography (Oct)

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