Data / Medical devices / United States / LV Liberty Vision
LV Liberty Vision: FDA-registered device maker in Portsmouth, NH, United States, 1 510(k) clearance
LV Liberty Vision is registered with the FDA (registration 3015042204) in Portsmouth, NH, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 29, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015042204
- Address
- 300 West Rd Ste 2, Portsmouth, NH, United States, 03801
- Owner or operator
- LV Liberty Vision (10059015)
- Roles
- Manufacturer
- First device listed
- November 30, 2021
- Registered through
- 2026
- Brand names listed
- LV Liberty Vision Model 1 90Yttrium Brachytherapy Source, LV Y-90 D10, LV Y-90 D6, LV iWand A Assembly Stand, LV iWand A10, LV iWand A6, LV iWand P Assembly Stand, LV iWand P10 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Source, Brachytherapy, Radionuclide | KXK | 2 | Manufacturer | accessdata.fda.gov |
| System, Applicator, Radionuclide, Manual | IWJ | 1 | 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 |
|---|---|---|---|---|---|---|
| May 29, 2020 | K193602 | LV Liberty Vision Model 1 90Yttrium Brachytherapy Source | KXK | Substantially Equivalent | Lv Liberty Vision Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Source, Brachytherapy, Radionuclide
- All makers of System, Applicator, Radionuclide, Manual
Updated May 29, 2020. 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.