I-Stethos Link
FDA 510(k) K022298 · Andromed, Inc.
510(k) numberK022298
Submission
- Device name
- I-Stethos Link
- Applicant
- Andromed, Inc.
Saint Laurent, Quebec, CA - Received
- July 16, 2002
- Decision date
- October 1, 2002
- Decision
- Substantially Equivalent (SESE)
- Type
- Abbreviated 510(k)
- Summary
- 510(k) statement 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 |
|---|---|---|
| K051779 | Androflow - Respiratory Rate MonitorBZQ · Abbreviated | 09/30/2005SE |
| K021389 | Biological Sound Monitor (BSM) SensorDQD · Abbreviated | 10/01/2002SE |
| K010729 | Agilent Electronic Stethoscope, Models M4532A and M4533ADQD · Traditional | 10/26/2001SE |
| K001306 | Stethos, Model Stxxyyzz or 001 XXX, Stethos Link, Model Slxxyyzz or 002 XXXDQD · Traditional | 07/20/2000SE |
Questions and answers
When was I-Stethos Link cleared by the FDA?
I-Stethos Link (K022298) received a 510(k) decision of Substantially Equivalent on October 1, 2002, 77 days after the submission was received.
What is the product code of K022298?
The FDA product code is DQD – Stethoscope, Electronic, a Class II (moderate risk) device regulated under 21 CFR 870.1875.