BECTON DICKINSON INTELLIPORT SYSTEM— 510(k) K141474
Substantially EquivalentBecton, Dickinson & CO
FDA 510(k) clearance K141474 for BECTON DICKINSON INTELLIPORT SYSTEM, Substantially Equivalent on 2014-12-18. Applicant: Becton, Dickinson & CO. Device class: 2.
Clearance details
- Applicant
- Becton, Dickinson & CO
- Product code
- Code PHC
- Device class
- Class 2
- Regulation
- 21 CFR 880.5725
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Diego, CA, US
Recent devices under product code PHC
view allMore clearances from Becton, Dickinson & CO
view all- K160164 — BD Veritor System for Rapid Detection of Flu A + B Labratory Kit
- K160161 — BD Veritor System for Rapid Detection of Flu A + B CLIA waived kit
- K140446 — BD PROBETEC CHLAMYDIA TRACHOMATIS (CT) QX AMPLIFIED DNA ASSAY
- K140448 — BD PROBETEC NEISSERIA GONORRHOEAE (GC) QX AMPLIFIED DNA ASSAY
- K140591 — BD PHASEAL CLOSED SYSTEM TRANSFER DEVICE - INJECTOR
Recalls naming K141474
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 K141474.
Data sourced from openFDA. This site is unofficial and independent of the FDA.