Cleared Traditional

Dr?s Finder NEO

K171867 · Good Doctors Co., Ltd. · Dental
Mar 2018
Decision
281d
Days
—
Risk

About This 510(k) Submission

K171867 is an FDA 510(k) clearance for the Dr?s Finder NEO, a Locator, Root Apex, submitted by Good Doctors Co., Ltd. (Incheon, KR). The FDA issued a Cleared decision on March 30, 2018, 281 days after receiving the submission on June 22, 2017. This device falls under the Dental review panel.

Submission Details

510(k) Number K171867 FDA.gov
FDA Decision Cleared SESE
Date Received June 22, 2017
Decision Date March 30, 2018
Days to Decision 281 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF

Device Classification

Product Code LQY — Locator, Root Apex
Device Class —

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