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

17HK700G-W

K Number: K180332 · Decision Jun 8, 2018
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
5
Review Days
122

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Basic Information

Device Name
17HK700G-W
K Number
K180332
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lg Electronics
Date Received
February 6, 2018
Decision Date
June 8, 2018
Product Code
MQB
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
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

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K Number Device Name
K191188 ASHK100G
K170984 LG BEAUTY LED MASK
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K133997 LG SMARTHEALTH