FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

R2GATE

K Number: K190096 · Decision Jun 26, 2019
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
16
Review Days
155

Basic Information

Device Name
R2GATE
K Number
K190096
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MegaGen Implant Co., Ltd.
Date Received
January 22, 2019
Decision Date
June 26, 2019
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
LLZ System, Image Processing, Radiological

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