Data / Medical devices / United States / Scientific Analytics/DARI Motion, Overland Park, KS USA
Scientific Analytics/DARI Motion, Overland Park, KS USA: FDA-registered device maker in Overland Park, KS, United States, 1 510(k) clearance
Scientific Analytics/DARI Motion, Overland Park, KS USA is registered with the FDA (registration 3015443141) in Overland Park, KS, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 7, 2019. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3015443141
- Address
- 9401 Indian Creek Parkway Suite 750, Overland Park, KS, United States, 66210
- Owner or operator
- DARI Motion, Inc. (10059957)
- Roles
- Manufacturer
- First device listed
- March 14, 2019
- Registered through
- 2026
- Brand names listed
- DARI Health
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Interactive Rehabilitation Exercise Devices | LXJ | 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 |
|---|---|---|---|---|---|---|
| March 7, 2019 | K180880 | DARI Health | LXJ | Substantially Equivalent | Scientific Analytics, Inc. | accessdata.fda.gov |
Compare with other makers
Updated March 7, 2019. 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.