Data / Medical devices / United States / Right Way Medical LLC
Right Way Medical LLC: FDA-registered device maker in Westerville, OH, United States, 1 510(k) clearance
Right Way Medical LLC is registered with the FDA (registration 3014383500) in Westerville, OH, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 14, 2021. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3014383500
- Address
- 835 Green Crest Dr, Westerville, OH, United States, 43081
- Owner or operator
- Right Way Medical LLC (10091338)
- Roles
- Complaint file establishment
- First device listed
- August 28, 2024
- Registered through
- 2027
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Set, Administration, Intravascular | FPA | 2 | Complaint file establishment | 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 |
|---|---|---|---|---|---|---|
| August 14, 2021 | K210381 | I.V. Administration Set | FPA | Substantially Equivalent | Bq Plus Medical Co., Ltd. | accessdata.fda.gov |
Compare with other makers
Updated August 14, 2021. 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.