Stethophone
K-Number: K240901 · 2024-09-19
ApplicantSparrow Acoustics, Inc.
Decision Date2024-09-19
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 2024-09-19 under approval number K240901. 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 2024-09-19. It is manufactured by Sparrow Acoustics, Inc.. The 510(k) number is K240901.
When was Stethophone approved by the FDA?
Stethophone received FDA 510(k) clearance on 2024-09-19, under approval number K240901.
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.