Data / Medical devices / United States / Analytics For Life Inc.
Analytics For Life Inc.: FDA-registered device maker in Bethesda, MD, United States, 3 510(k) clearances
Analytics For Life Inc. is registered with the FDA (registration 3033300766) in Bethesda, MD, United States. It lists 3 device types. The FDA files 3 510(k) clearances under its listings, the newest dated July 26, 2026. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3033300766
- Address
- 3 Bethesda Metro Center, Suite 700, Bethesda, MD, United States, 20814
- Owner or operator
- Analytics for Life Inc. (10089389)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- December 4, 2023
- Registered through
- 2026
- Brand names listed
- CorVista System, CorVista System with PH Add-On, CorVista® System with PCWP Add-On
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Computer, Diagnostic, Programmable | DQK | 2 | Manufacturer | accessdata.fda.gov |
| Coronary Artery Disease Machine Learning-Based Notification Software | QXX | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Pulmonary Hypertension Machine Learning-Based Notification Software | SAT | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| July 26, 2026 | K253576 | CorVista System® with PCWP Add-On | DQK | Substantially Equivalent | Analytics For Life, Inc. | accessdata.fda.gov |
| April 5, 2024 | K233666 | CorVista System with PH Add-On | SAT | Substantially Equivalent | Analytics For Life, Inc. | accessdata.fda.gov |
| September 8, 2023 | K232686 | CorVista® System | QXX | Substantially Equivalent | Corvista Health, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Computer, Diagnostic, Programmable
- All makers of Pulmonary Hypertension Machine Learning-Based Notification Software
Updated July 26, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.