BD MiniDraw Capillary Blood Collection System with BD MiniDraw SST Capillary Blood Collection Tube— 510(k) K230391
Substantially EquivalentBecton, Dickinson and Company
FDA 510(k) clearance K230391 for BD MiniDraw Capillary Blood Collection System with BD MiniDraw SST Capillary Blood Collection Tube, Substantially Equivalent on 2023-12-01. Applicant: Becton, Dickinson and Company.
Clearance details
- Applicant
- Becton, Dickinson and Company
- Product code
- Code JKA
- Advisory panel
- Clinical Chemistry
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Franklin Lakes, NJ, US
Adverse events under product code JKA
product code JKA- Injury
- 455
- Malfunction
- 26,686
- Other
- 4
- Total
- 27,145
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.