Data / Medical devices / United States / Foresight Imaging, LLC
Foresight Imaging, LLC: FDA-registered device maker in Chelmsford, MA, United States, 1 510(k) clearance
Foresight Imaging, LLC is registered with the FDA (registration 1064588) in Chelmsford, MA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 22, 2000. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1064588
- FEI number
- 3003063996
- Address
- 1 Executive Dr Ste 202, Chelmsford, MA, United States, 01824
- Owner or operator
- FORESIGHT IMAGING, LLC (9078644)
- Roles
- Manufacturer
- First device listed
- March 18, 2004
- Registered through
- 2026
- Brand names listed
- TIMS
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 |
|---|---|---|---|---|---|---|
| November 22, 2000 | K001947 | T.I.M.S., VERSION 2.00 | LLZ | Substantially Equivalent | Total Medical Information Management Systems, Inc. | accessdata.fda.gov |
Compare with other makers
Updated November 22, 2000. 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.