Data / Medical devices / United States / US Vascular
US Vascular: FDA-registered device maker in Beaverton, OR, United States, 1 510(k) clearance
US Vascular is registered with the FDA (registration 3010089756) in Beaverton, OR, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 27, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3010089756
- Address
- 7874 SW Nimbus Avenue, Beaverton, OR, United States, 97008
- Owner or operator
- US Vascular (10045849)
- Roles
- Manufacturer
- First device listed
- January 6, 2014
- Registered through
- 2026
- Brand names listed
- VascuLab 4040, VascuLab 4040 GSX, VascuLab 4043
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Transducer, Ultrasonic | JOP | 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 |
|---|---|---|---|---|---|---|
| September 27, 2013 | K131860 | VASCULAB VL4000 PHOTOPLETHYSMOGRAPH WITH PULSE VOLUME RECORDING | JOP | Substantially Equivalent | Us Vascular, LLC | accessdata.fda.gov |
Compare with other makers
Updated September 27, 2013. 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.