Feelix Stethoscope
K-Number: K200862 · 2020-09-14
ApplicantSonavi Labs, Inc.
Decision Date2020-09-14
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Feelix Stethoscope is a medical device manufactured by Sonavi Labs, Inc.. It received FDA 510(k) clearance on 2020-09-14 under approval number K200862. 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 Feelix Stethoscope?
Feelix Stethoscope is a medical device that received FDA 510(k) clearance on 2020-09-14. It is manufactured by Sonavi Labs, Inc.. The 510(k) number is K200862.
When was Feelix Stethoscope approved by the FDA?
Feelix Stethoscope received FDA 510(k) clearance on 2020-09-14, under approval number K200862.
What company makes Feelix Stethoscope?
Feelix Stethoscope is manufactured by Sonavi Labs, Inc..
What is the FDA product code for Feelix Stethoscope?
The FDA product code for Feelix Stethoscope is DQD.
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.