Data / Medical devices / United States / Medstrat
Medstrat: FDA-registered device maker in Downers Grove, IL, United States, 1 510(k) clearance
Medstrat is registered with the FDA (registration 3003574171) in Downers Grove, IL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated July 14, 2005. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3003574171
- Address
- 1901 Butterfield RD. Suite 600, Downers Grove, IL, United States, 60515
- Owner or operator
- MEDSTRAT (9048078)
- Roles
- Manufacturer
- First device listed
- August 15, 2013
- Registered through
- 2027
- Brand names listed
- Joints
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| System, Image Processing, Radiological | LLZ | 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 |
|---|---|---|---|---|---|---|
| July 14, 2005 | K051745 | ECHOSYSTEM | LLZ | Substantially Equivalent | Medstrat, Inc. | accessdata.fda.gov |
Compare with other makers
Updated July 14, 2005. 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.