Tyto Stethoscope
K-Number: K160401 · 2016-10-19
ApplicantTyto Care , Ltd.
Decision Date2016-10-19
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Tyto Stethoscope is a medical device manufactured by Tyto Care , Ltd.. It received FDA 510(k) clearance on 2016-10-19 under approval number K160401. 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?
Tyto Stethoscope is a medical device that received FDA 510(k) clearance on 2016-10-19. It is manufactured by Tyto Care , Ltd.. The 510(k) number is K160401.
When was Tyto Stethoscope approved by the FDA?
Tyto Stethoscope received FDA 510(k) clearance on 2016-10-19, under approval number K160401.
What company makes Tyto Stethoscope?
Tyto Stethoscope is manufactured by Tyto Care , Ltd..
What is the FDA product code for Tyto Stethoscope?
The FDA product code for Tyto Stethoscope 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.