BIOPLEX VASCULITIS KIT— 510(k) K072358
Substantially EquivalentBio-Rad Laboratories
FDA 510(k) clearance K072358 for BIOPLEX VASCULITIS KIT, Substantially Equivalent on 2007-10-31. Applicant: Bio-Rad Laboratories.
Clearance details
- Applicant
- Bio-Rad Laboratories
- Product code
- Code MVJ
- Advisory panel
- Immunology
- 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.