Alere, San Diego, Dba Biosite INcorporated, Dba IN
Country not established
- Devices
- 1
What Alere, San Diego, Dba Biosite INcorporated, Dba IN makes
The company produces multi-analyte control materials and calibration verification reagents for lipid testing, designed to validate the accuracy and performance of diagnostic assays in clinical laboratories.
These products are classified as Class I medical devices under FDA regulations and are supported by 510(k) clearances. The company is headquartered in the United States.
Catalogue
Lipid Controls; Multi- Analyte Control; Multi-Analyte Calibration Verification Materials Ref K102700
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Alere, San Diego, Dba Biosite INcorporated, Dba IN have in the registry?
The registry currently lists 1 device for Alere, San Diego, Dba Biosite INcorporated, Dba IN. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alere, San Diego, Dba Biosite INcorporated, Dba IN's devices?
Among its 1 most recently registered device, Alere, San Diego, Dba Biosite INcorporated, Dba IN has devices listed in FDA 510(k) (1 device).
What risk classes do Alere, San Diego, Dba Biosite INcorporated, Dba IN's devices fall under?
Among its 1 most recently registered device, the classes recorded for Alere, San Diego, Dba Biosite INcorporated, Dba IN's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Alere, San Diego, Dba Biosite INcorporated, Dba IN in the registry?
The most recently registered devices listed for Alere, San Diego, Dba Biosite INcorporated, Dba IN include LIPID CONTROLS; MULTI- ANALYTE CONTROL; MULTI-ANALYTE CALIBRATION VERIFICATION MATERIALS.