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FDA 510(k)

Dr’s Finder NEO

K-Number: K171867 · 2018-03-30

ApplicantGood Doctors Co., Ltd.
Decision Date2018-03-30
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

Dr’s Finder NEO is a medical device manufactured by Good Doctors Co., Ltd.. It received FDA 510(k) clearance on 2018-03-30 under approval number K171867. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dr’s Finder NEO?

Dr’s Finder NEO is a medical device that received FDA 510(k) clearance on 2018-03-30. It is manufactured by Good Doctors Co., Ltd.. The 510(k) number is K171867.

When was Dr’s Finder NEO approved by the FDA?

Dr’s Finder NEO received FDA 510(k) clearance on 2018-03-30, under approval number K171867.

What company makes Dr’s Finder NEO?

Dr’s Finder NEO is manufactured by Good Doctors Co., Ltd..

What is the FDA product code for Dr’s Finder NEO?

The FDA product code for Dr’s Finder NEO is LQY.

Other Devices by Good Doctors Co., Ltd.

K151274Dr's Finder K173157Dr's Light2 K183471IC-WHCD100 (Inspire) K223507CL-DP40 (Dr’s Light PRIME), CL-DP40 (Dr’s Light CHOICE)

Related Devices (Code: LQY)

K151274Dr's FinderGood Doctors Co., Ltd. K181087Apex Locator, DPEX IIIGuilin Woodpecker Medical Instrument Co., Ltd. K191806Propex IQ Apex LocatorDentsply Sirona K210789EQ-PEXMeta Systems Co., Ltd. K203836BOMEDENT Apex locator, WISMY Apex locatorChangzhou Bomedent Medical Technology Co.,Ltd K212178Root Apex LocatorFoshan Coxo Medical Instrument Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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