Stethophone
K-Number: K231551 · 2023-10-12
ApplicantSparrow Acoustics, Inc.
Decision Date2023-10-12
Product CodeDQD
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Stethophone is a medical device manufactured by Sparrow Acoustics, Inc.. It received FDA 510(k) clearance on 2023-10-12 under approval number K231551. 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 Stethophone?
Stethophone is a medical device that received FDA 510(k) clearance on 2023-10-12. It is manufactured by Sparrow Acoustics, Inc.. The 510(k) number is K231551.
When was Stethophone approved by the FDA?
Stethophone received FDA 510(k) clearance on 2023-10-12, under approval number K231551.
What company makes Stethophone?
Stethophone is manufactured by Sparrow Acoustics, Inc..
What is the FDA product code for Stethophone?
The FDA product code for Stethophone is DQD.
Other Devices by Sparrow Acoustics, Inc.
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.