Data / Medical devices / United States / Segami Corporation
Segami Corporation: FDA-registered device maker in Columbia, MD, United States, 1 510(k) clearance
Segami Corporation is registered with the FDA (registration 3003370689) in Columbia, MD, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated August 31, 2007. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3003370689
- Address
- 8325 Guilford Rd Ste E, Columbia, MD, United States, 21046
- Owner or operator
- SEGAMI CORPORATION (9045043)
- Roles
- Manufacturer
- First device listed
- July 21, 2010
- Registered through
- 2027
- Brand names listed
- Oasis
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 |
|---|---|---|---|---|---|---|
| August 31, 2007 | K071584 | OASIS RELEASE 1.0 | LLZ | Substantially Equivalent | Segami Corporation | accessdata.fda.gov |
Compare with other makers
Updated August 31, 2007. 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.