Data / Medical devices / United States / Seca Corp.
Seca Corp.: FDA-registered device maker in Chino, CA, United States, 1 510(k) clearance
Seca Corp. is registered with the FDA (registration 1120986) in Chino, CA, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 23, 2020. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 1120986
- Address
- 13601 Benson Ave, Chino, CA, United States, 91710
- Owner or operator
- SECA (8010918)
- Roles
- Complaint file establishment
- First device listed
- May 31, 2018
- Registered through
- 2027
- Brand names listed
- seca analytics 125, seca mBCA 525, seca mVSA 535
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Analyzer, Body Composition, Exempt | PUH | 2 | Complaint file establishment | accessdata.fda.gov |
| Continuous Measurement Thermometer | FLL | 2 | Complaint file establishment | accessdata.fda.gov |
| Oximeter | DQA | 2 | Complaint file establishment | accessdata.fda.gov |
| System, Measurement, Blood-Pressure, Non-Invasive | DXN | 2 | Complaint file establishment | 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 |
|---|---|---|---|---|---|---|
| January 23, 2020 | K192092 | Seca Medical Vital Signs Analyzer 535, Seca mVSA 535, Seca mVSA, Seca 535 | DXN | Substantially Equivalent | Seca GmbH & Co. KG | accessdata.fda.gov |
Compare with other makers
- All makers of Oximeter
- All makers of Continuous Measurement Thermometer
- All makers of System, Measurement, Blood-Pressure, Non-Invasive
- All makers of Analyzer, Body Composition, Exempt
Updated January 23, 2020. 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.