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U.S. Department of Health and Human Services

510(k) Premarket Notification

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Device Classification Name locator, root apex
510(k) Number K171867
Device Name Dr’s Finder NEO
Good Doctors Co.,Ltd.
#208, B-Dong, 283 Bupyeong-Daero, Bupyeong-Gu
Incheon,  KR 21315
Applicant Contact Sungro Joo
LK Consulting Group USA, Inc.
690 Roosevelt,
Irvine,  CA  92620
Correspondent Contact Priscilla Chung
Classification Product Code
Date Received06/22/2017
Decision Date 03/30/2018
Decision Substantially Equivalent (SESE)
510k Review Panel Dental
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No