LEUCOPREP(R) BRAND CELL SEPARAT TUBE W/SODIUM CITR— 510(k) K911731
Substantially EquivalentBd Becton Dickinson Vacutainer Systems Preanalytic
FDA 510(k) clearance K911731 for LEUCOPREP(R) BRAND CELL SEPARAT TUBE W/SODIUM CITR, Substantially Equivalent on 1992-12-15. Applicant: Bd Becton Dickinson Vacutainer Systems Preanalytic. Device class: 1.
Clearance details
- Applicant
- Bd Becton Dickinson Vacutainer Systems Preanalytic
- Product code
- Code JCF
- Device class
- Class 1
- Regulation
- 21 CFR 864.8500
- Advisory panel
- Hematology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Franklin Lakes, NJ, US
Recent devices under product code JCF
view allMore clearances from Bd Becton Dickinson Vacutainer Systems Preanalytic
view allRecalls naming K911731
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K911731.
Data sourced from openFDA. This site is unofficial and independent of the FDA.