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FDA 510(k) Application Details - K232127
Device Classification Name
More FDA Info for this Device
510(K) Number
K232127
Device Name
21HQ513D, 32HL512D, 31HN713D, 32HQ713D
Applicant
LG Electronics Inc.
168, Suchul-daero
Gumi-si 39368 KR
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Contact
Daseul An
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Regulation Number
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Classification Product Code
PGY
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More FDA Info for this Product Code
Date Received
07/17/2023
Decision Date
08/15/2023
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
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