Data / Medical devices / United States / Pedia
Pedia: FDA-registered device maker in Fairfax, VA, United States, 1 510(k) clearance
Pedia is registered with the FDA (registration 3014729687) in Fairfax, VA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated September 25, 2018. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014729687
- Address
- 2804 Albany Court, Fairfax, VA, United States, 22031
- Owner or operator
- PeDIA (10061544)
- Roles
- Specification developer
- First device listed
- October 28, 2019
- Registered through
- 2026
- Brand names listed
- PeDIA
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bag, Reservoir | BTC | 1 | Specification developer | 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 25, 2018 | K181424 | PeDIA | BTC | Substantially Equivalent | Pedia, LLC | accessdata.fda.gov |
Compare with other makers
Updated September 25, 2018. 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.