Tyto Stethoscope (G3)
K-Number: K252089 · 2026-03-12
Device Summary
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. The listed applicant is Tyto Care , Ltd.. The 510(k) number is K252089.
When did Tyto Stethoscope (G3) receive FDA 510(k) clearance?
Tyto Stethoscope (G3) received FDA 510(k) clearance on 2026-03-12, under 510(k) number K252089.
Who is the listed applicant for Tyto Stethoscope (G3)?
The FDA 510(k) record lists Tyto Care , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Tyto Stethoscope (G3)?
The FDA product code for Tyto Stethoscope (G3) is DQD.
Other records listing Tyto Care , 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: DQD)
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.