Data / Medical devices / United States / Thinking Systems Corp.
Thinking Systems Corp.: FDA-registered device maker in Saint Petersburg, FL, United States, 1 510(k) clearance
Thinking Systems Corp. is registered with the FDA (registration 1066247) in Saint Petersburg, FL, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated April 3, 2001. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1066247
- FEI number
- 3003261709
- Address
- 750 94TH Ave., N. Suite 211, Saint Petersburg, FL, United States, 33702
- Owner or operator
- THINKING SYSTEMS CORP. (9044519)
- Roles
- Manufacturer
- First device listed
- January 26, 2001
- Registered through
- 2026
- Brand names listed
- MDSTATION, NUPAX, THINKINGNET
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Digital Image Storage, Radiological | LMB | 1 | Manufacturer | accessdata.fda.gov |
| System, Digital Image Communications, Radiological | LMD | 1 | Manufacturer | accessdata.fda.gov |
| 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 |
|---|---|---|---|---|---|---|
| April 3, 2001 | K010271 | THINKINGNET | LLZ | Substantially Equivalent | Thinking Systems Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Digital Image Storage, Radiological
- All makers of System, Image Processing, Radiological
- All makers of System, Digital Image Communications, Radiological
Updated April 3, 2001. 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.