Stethophone
FDA 510(k) K240901 · Sparrow Acoustics, Inc.
510(k) numberK240901
Submission
- Device name
- Stethophone
- Applicant
- Sparrow Acoustics, Inc.
Lucasville, CA - Received
- April 2, 2024
- Decision date
- September 19, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DQD – Stethoscope, Electronic
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1875
- Specialty
- Cardiovascular
Other 510(k)s with product code DQD
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K261494 | Smart Wireless Stethoscope (STEMO310);Smart Wireless Stethoscope (STEMO710);Smart…DQD · Traditional | Shanghai Hulu Devices Co., Ltd. | 07/31/2026SE |
| K261694 | CORE 300 Digital StethoscopeDQD · Traditional | Eko Health, Inc. | 07/23/2026SE |
| K252915 | AiSteth®DQD · Traditional | Ai Health Highway India Pvt., Ltd. | 05/22/2026SE |
| K252089 | Tyto Stethoscope (G3)DQD · Traditional | Tyto Care , Ltd. | 03/12/2026SE |
| K252076 | Kneevoice Cartilage Evaluation System (750-3600-001)DQD · Traditional | Kneevoice, Inc. | 02/06/2026SE |
| K252284 | eMurmur Heart AIDQD · Traditional | Csd Labs | 12/19/2025SE |
| K252595 | Stethophone ProDQD · Special | Sparrow Acoustics, Inc. | 09/12/2025SE |
| K251494 | Eko Foundation Analysis Software with Transformers (EFAST)DQD · Traditional | Eko Health, Inc. | 08/12/2025SE |
| K242971 | AccurSound Electronic Stethoscope (AS101)DQD · Traditional | Heroic Faith International , Ltd. | 11/25/2024SE |
| K233313 | Keikku Electronic stethoscopeDQD · Traditional | Lapsi Health Holding B.V. | 04/10/2024SE |
More from Lapsi Health Holding B.V.
Questions and answers
When was Stethophone cleared by the FDA?
Stethophone (K240901) received a 510(k) decision of Substantially Equivalent on September 19, 2024, 170 days after the submission was received.
What is the product code of K240901?
The FDA product code is DQD – Stethoscope, Electronic, a Class II (moderate risk) device regulated under 21 CFR 870.1875.