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FDA 510(k)

Tyto Stethoscope (G3)

K-Number: K252089 · 2026-03-12

Decision Date2026-03-12
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Tyto Stethoscope (G3) is the device name listed in this FDA 510(k) record. The listed applicant is Tyto Care , Ltd.. It received FDA 510(k) clearance on 2026-03-12 under 510(k) 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. 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.

View all 9 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.