Devices · Tyto Care , Ltd.

Tyto Stethoscope (G3)

Tyto Care , Ltd. is listed for Tyto Stethoscope (G3) (K252089). The FDA list gives March 12, 2026 as the date of the final decision. The lead panel is Cardiovascular, and the database link on the FDA list is the 510(k) pathway. The primary product code on the FDA list is DQD. openFDA did not return a classification record for that code in this copy of the data. openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K252089

Official FDA database record

Date of final decision

March 12, 2026

Company on the FDA list

Tyto Care , Ltd.

Lead panel

Cardiovascular

Primary product code

DQD

openFDA device name for the code

Stethoscope, Electronic

Device class

2

Regulation number

870.1875

openFDA decision description

Substantially Equivalent

openFDA decision code

SESE

Statement or summary label

Summary