510(k) K260780
- Device
- HeartFocus
- Applicant
- Deski
- 510(k) number
- K260780
- Product code
- QJU
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 2026-06-03
- Date received
- 2026-03-10
- Regulation
- 892.2100
- Classification name
- Image Acquisition And/Or Optimization Guided By Artificial Intelligence
- Medical specialty
- Radiology
- Review panel
- Radiology
- Device class
- 2
- Clearance type
- Special
- Statement or summary
- Summary
- Third party reviewed
- N
Applicant Contact#
- Contact
- Kelly Porfirio
- Address
- 2 Pl. De La Bourse Bordeaux FR 33000 33000
FDA Registration Numbers#
- 3029923647
- 3032008018
- 3040362673
Source Documents#
Other 510(k) Records For Product Code QJU#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K251416 | UltraSight Guidance | Ultrasight , Ltd. | 2025-12-17 |
| K242807 | HeartFocus (V.1.1.1) | Deski | 2025-04-04 |
| K243065 | Cardiac Guidance | Caption Health, Inc. | 2025-01-15 |
| K223347 | UltraSight AI Guidance | Ultrasight, Inc. | 2023-07-24 |
| K201992 | Caption Guidance | Caption Health | 2020-09-18 |
| K200755 | Caption Guidance | Caption Health | 2020-04-16 |
| DEN190040 | Caption Guidance | Bay Labs, Inc. | 2020-02-07 |