← Back to catalogue

Dr’s Finder NEO

FDA 510(k)EUDAMED

U (US FDA 510(k))

510(k) K171867

by Good Doctors Co., Ltd.

Identifiers

510(k) Number
K171867 FDA 510(k)
FDA Product Code
LQY FDA 510(k)

Classification

Device Class
U FDA 510(k)
Advisory Committee
Unknown FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Dr’s Finder NEO by Good Doctors Co., Ltd. — U — MDR, FDA_510K — listed in FDA 510(k), EUDAMED — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

MDR

United States Active

FDA_510K

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA 510(k) K171867 24 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced May 18, 2026