BIOPLEX 2200 MMRV IGG— 510(k) K091616
Substantially EquivalentBio-Rad Laboratories
FDA 510(k) clearance K091616 for BIOPLEX 2200 MMRV IGG, Substantially Equivalent on 2010-03-29. Applicant: Bio-Rad Laboratories.
Clearance details
- Applicant
- Bio-Rad Laboratories
- Product code
- Code OPL
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Redmond, WA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.