Midmark Iqecg
FDA 510(k) K103640 · Brentwood Medical Technology Corp.
510(k) numberK103640
Submission
- Device name
- Midmark Iqecg
- Applicant
- Brentwood Medical Technology Corp.
Irvine, CA, US - Received
- December 13, 2010
- Decision date
- March 22, 2011
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- DPS – Electrocardiograph
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.2340
- Specialty
- Cardiovascular
Other 510(k)s with product code DPS
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K252463 | SE-1202 Series Electrocardiograph (Model: SE-1202, SE-1202E)DPS · Traditional | Edan Instruments, Inc. | 07/02/2026SE |
| K251670 | MAC 7 Resting ECG Analysis SystemDPS · Traditional | Ge Medical Systems Information Technologies, Inc. | 01/26/2026SE |
| K252361 | AccurECG Analysis System (v2.0)DPS · Traditional | Accurkardia, Inc. | 12/22/2025SE |
| K252474 | Withings BeamO (SCT02)DPS · Traditional | Withings | 11/10/2025SE |
| K250569 | Cardiologs Holter PlatformDPS · Traditional | Philips France Commercial | 08/06/2025SE |
| K243252 | ZBPro DiagnosticDPS · Traditional | Zbeats, Inc. | 07/10/2025SE |
| K243305 | Masimo W1DPS · Traditional | Masimo Corporation | 04/03/2025SE |
| K241217 | CloudHRV System (100-01-001)DPS · Traditional | Inmedix, Inc. | 01/16/2025SE |
| K241556 | Cardiac Workstation (5000); Cardiac Workstation (7000)DPS · Traditional | Philips Medizin Systeme Böblingen GmbH | 12/17/2024SE |
| K240229 | Masimo W1DPS · Traditional | Masimo Corporation | 08/08/2024SE |
More from Masimo Corporation
| 510(k) | Device | Decision |
|---|---|---|
| K100913 | Iqvitals and Iqvitals SystemDXN · Traditional | 05/26/2010SE |
| K052898 | Iqmark Ez StressDPS · Traditional | 03/28/2006SE |
| K031466 | Iqmark Digital HolterMLO · Special | 06/11/2003SE |
| K013717 | Brentwood Real Time ST and Arrhythmia Analysis Software LibraryDPS · Traditional | 02/06/2002SE |
| K010505 | Telemed 12 Lead Resting ECG Analysis LibraryDPS · Special | 03/09/2001SE |
| K002499 | Brentwood Iqmark Digital Spirometer (Includes Disposable Pneumotach Mouthpieces and…BZG · Traditional | 11/08/2000SE |
Questions and answers
When was Midmark Iqecg cleared by the FDA?
Midmark Iqecg (K103640) received a 510(k) decision of Substantially Equivalent on March 22, 2011, 99 days after the submission was received.
What is the product code of K103640?
The FDA product code is DPS – Electrocardiograph, a Class II (moderate risk) device regulated under 21 CFR 870.2340.