Sparrow Acoustics, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Sparrow Acoustics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Stethophone Pro, Stethophone, Stethophone
4
Total
4
Cleared
0
Denied
Sparrow Acoustics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Lucasville, CA.
Latest FDA clearance: Sep 2025. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Sparrow Acoustics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sparrow Acoustics, Inc.
4 devices