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FDA 510(k)

Dr's Finder

K-Number: K151274 · 2016-02-04

ApplicantGood Doctors Co., Ltd.
Decision Date2016-02-04
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

Dr's Finder is a medical device manufactured by Good Doctors Co., Ltd.. It received FDA 510(k) clearance on 2016-02-04 under approval number K151274. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dr's Finder?

Dr's Finder is a medical device that received FDA 510(k) clearance on 2016-02-04. It is manufactured by Good Doctors Co., Ltd.. The 510(k) number is K151274.

When was Dr's Finder approved by the FDA?

Dr's Finder received FDA 510(k) clearance on 2016-02-04, under approval number K151274.

What company makes Dr's Finder?

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

What is the FDA product code for Dr's Finder?

The FDA product code for Dr's Finder is LQY.

Other Devices by Good Doctors Co., Ltd.

K173157Dr's Light2 K171867Dr’s Finder NEO K183471IC-WHCD100 (Inspire) K223507CL-DP40 (Dr’s Light PRIME), CL-DP40 (Dr’s Light CHOICE)

Related Devices (Code: LQY)

K181087Apex Locator, DPEX IIIGuilin Woodpecker Medical Instrument Co., Ltd. K171867Dr’s Finder NEOGood Doctors 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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