RUBELLA IGG ANTIBODY ELISA TEST SYS— 510(k) K841200
Substantially EquivalentOrtho Diagnostic Systems, Inc.
FDA 510(k) clearance K841200 for RUBELLA IGG ANTIBODY ELISA TEST SYS, Substantially Equivalent on 1984-05-21. Applicant: Ortho Diagnostic Systems, Inc..
Clearance details
- Applicant
- Ortho Diagnostic Systems, Inc.
- Product code
- Code LFX
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Carpinteria, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.