FDA applicant
Sparrow Acoustics, Inc.
FDA records 4 decisions for Sparrow Acoustics, Inc. (Lucasville, CA) from 2023 to 2025: 4 510(k) clearances. All are in product code DQD (Stethoscope, Electronic). Since 2016 its 510(k)s took a median of 153 days from receipt to decision, against 132 for FDA’s reviews in the same codes and years. Its devices cite 7 predicates, 3 of them its own earlier devices. No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Sparrow Acoustics, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2025
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2023.
Planning a device like Sparrow Acoustics, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) Report