Signal
FDA 510(k) K090493 · Zargis Medical Corp.
510(k) numberK090493
Submission
- Device name
- Signal
- Applicant
- Zargis Medical Corp.
Princeton, NJ, US - Received
- February 25, 2009
- Decision date
- August 7, 2009
- 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 |
| K240901 | StethophoneDQD · Traditional | Sparrow Acoustics, Inc. | 09/19/2024SE |
More from Sparrow Acoustics, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K083309 | Zargis Acoustic Cardioscan, Version 9.33DQD · Special | 02/13/2009SE |
| K060197 | Zargis Acoustic Cardioscan (Zac), Model Zac 6.28DQD · Special | 03/29/2006SE |
| K042128 | Modification to Zargis Acoustic Cardioscan (Zac)DQD · Special | 09/08/2004SE |
| K031517 | Zargis Acoustic CardioscanDQD · Traditional | 05/26/2004SE |
Questions and answers
When was Signal cleared by the FDA?
Signal (K090493) received a 510(k) decision of Substantially Equivalent on August 7, 2009, 163 days after the submission was received.
What is the product code of K090493?
The FDA product code is DQD – Stethoscope, Electronic, a Class II (moderate risk) device regulated under 21 CFR 870.1875.