Tyto Stethoscope (G3)
K-Number: K252089 · 2026-03-12
ApplicantTyto Care , Ltd.
Decision Date2026-03-12
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Tyto Stethoscope (G3) is a medical device manufactured by Tyto Care , Ltd.. It received FDA 510(k) clearance on 2026-03-12 under approval number K252089. The device is classified under product code DQD. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Tyto Stethoscope (G3)?
Tyto Stethoscope (G3) is a medical device that received FDA 510(k) clearance on 2026-03-12. It is manufactured by Tyto Care , Ltd.. The 510(k) number is K252089.
When was Tyto Stethoscope (G3) approved by the FDA?
Tyto Stethoscope (G3) received FDA 510(k) clearance on 2026-03-12, under approval number K252089.
What company makes Tyto Stethoscope (G3)?
Tyto Stethoscope (G3) is manufactured by Tyto Care , Ltd..
What is the FDA product code for Tyto Stethoscope (G3)?
The FDA product code for Tyto Stethoscope (G3) is DQD.
Other Devices by Tyto Care , Ltd.
Related Devices (Code: DQD)
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.