BIOPLEX 2200 EBV IGM KIT— 510(k) K123021
Substantially EquivalentBio-Rad Laboratories
FDA 510(k) clearance K123021 for BIOPLEX 2200 EBV IGM KIT, Substantially Equivalent on 2012-11-02. Applicant: Bio-Rad Laboratories.
Clearance details
- Applicant
- Bio-Rad Laboratories
- Product code
- Code LJN
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Benicia, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.