Dr’s Finder NEO
K-Number: K171867 · 2018-03-30
Device Summary
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. The listed applicant is Good Doctors Co., Ltd.. The 510(k) number is K171867.
When did Dr’s Finder NEO receive FDA 510(k) clearance?
Dr’s Finder NEO received FDA 510(k) clearance on 2018-03-30, under 510(k) number K171867.
Who is the listed applicant for Dr’s Finder NEO?
The FDA 510(k) record lists Good Doctors Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Dr’s Finder NEO?
The FDA product code for Dr’s Finder NEO is LQY.
Other records listing Good Doctors Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: LQY)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.