Drs Finder NEO— 510(k) K171867

Name: FDA 510(k) clearance K171867
Creator: U.S. Food and Drug Administration
Published: 2018-03-30

Substantially Equivalent

Good Doctors Co., Ltd.

FDA 510(k) clearance K171867 for Drs Finder NEO, Substantially Equivalent on 2018-03-30. Applicant: Good Doctors Co., Ltd.. Device class: Unclassified.

Clearance details

Applicant: Good Doctors Co., Ltd.
Product code: Code LQY
Device class: Unclassified
Advisory panel: Unknown
Date received: 2017-06-22
Decision date: 2018-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Incheon, KR

Download summary PDF View on FDA.gov ↗

Recent devices under product code LQY

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K242765 — Electronic Apex Locator (Alpha Apex I)2025-01-17
K231990 — Apex Locator2024-02-13
K232717 — Apex Locator (AL-Pex), Apex Locator (AL-Pex+)2023-12-22

More clearances from Good Doctors Co., Ltd.

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K223507 — CL-DP40 (Drs Light PRIME), CL-DP40 (Drs Light CHOICE)2023-08-04
K183471 — IC-WHCD100 (Inspire)2020-07-02
K173157 — Dr's Light22018-05-29
K151274 — Dr's Finder2016-02-04
K093751 — CL-DC20, CL-DC212010-02-24

Adverse events under product code LQY

product code LQY

Malfunction: 504
Total: 504

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.