Data / Medical devices / United States / Vista AI Inc.
Vista AI Inc.: FDA-registered device maker in Redwood City, CA, United States, 1 510(k) clearance
Vista AI Inc. is registered with the FDA (registration 3011767965) in Redwood City, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 25, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3011767965
- Address
- 702 Marshall St Ste 280, Redwood City, CA, United States, 94063
- Owner or operator
- Vista AI, Inc. (10049792)
- Roles
- Manufacturer
- First device listed
- July 30, 2015
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Nuclear Magnetic Resonance Imaging | LNH | 2 | 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 |
|---|---|---|---|---|---|---|
| June 25, 2014 | K133848 | RTHAWK, RTHAWK, OR HEARTVISTA WORKSTATION WITH RTHAWK | LNH | Substantially Equivalent | Heartvista, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 25, 2014. 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.