MODIFICATION TO DUET SYSTEM— 510(k) K050840
Substantially EquivalentBioview , Ltd.
FDA 510(k) clearance K050840 for MODIFICATION TO DUET SYSTEM, Substantially Equivalent on 2005-08-16. Applicant: Bioview , Ltd..
Clearance details
- Applicant
- Bioview , Ltd.
- Product code
- Code JOY
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ramat-Gan, IL
Data sourced from openFDA. This site is unofficial and independent of the FDA.