BBL DIRECTIGEN MENINGITIS TEST KIT— 510(k) K821266
Substantially EquivalentBd Becton Dickinson Vacutainer Systems Preanalytic
FDA 510(k) clearance K821266 for BBL DIRECTIGEN MENINGITIS TEST KIT, Substantially Equivalent on 1982-06-01. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic.
Clearance details
- Applicant
- Bd Becton Dickinson Vacutainer Systems Preanalytic
- Product code
- Code GRP
- Advisory panel
- Microbiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Washington, DC, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.