AXSYM RUBELLA IGG ANTIBODY ASSAY— 510(k) K954045
Substantially EquivalentAbbott Laboratories
FDA 510(k) clearance K954045 for AXSYM RUBELLA IGG ANTIBODY ASSAY, Substantially Equivalent on 1996-09-24. Applicant: Abbott Laboratories.
Clearance details
- Applicant
- Abbott Laboratories
- Product code
- Code LFX
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Abbott Park, IL, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.