510(k) K160657 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
BD Vacutainer Barricor Lithium Heparin Plasma Blood Collection Tube
| Applicant | Becton, Dickinson and Company, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Sep 23, 2016 |
| Received | Mar 8, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160657
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 22, 2018 | Becton Dickinson & Company BD Vacutainer Lithium Heparin Green Top Tube; Catalog Numbers: 1. 366664 (UDI: 50382903666640); 2. 367884 (UDI: 50382903678841); 3. 367886 (UDI: 50382903678865); 4. 368040 (UDI: 50382903680400); 5. 36 Terminated |
JKA | None listed |
| Sep 18, 2017 | Becton Dickinson & Company BD Vacutainer Barricor" Lithium Heparin Plasma Blood Collection Tubes for Invitro Diagnostic Use, Catalog Numbers: 365043, 365044, 365045 & 365047
Used to collect, separate, process, transport and s Terminated |
JKA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.