510(k) K901449 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
VACUTAINER PLUS WITH HEMOGARD CLOSURE
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Aug 9, 1990 |
| Received | Mar 28, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901449
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 12, 2019 | Becton Dickinson & Company BD Vacutainer Lithium HeparinN (LH) 37 USP Units Blood Collection Tubes, Catalog Number 366664 Terminated |
JKA | None listed |
| Jun 12, 2019 | Becton Dickinson & Company BD Vacutainer Lithium HeparinN (LH) 56 USP Units Blood Collection Tubes, Catalog Number 366667 Terminated |
JKA | None listed |
| Jun 12, 2019 | Becton Dickinson & Company BD Vacutainer Lithium HeparinN (LH) 158 USP Units Blood Collection Tubes, Catalog Number 367880 Terminated |
JKA | None listed |
| Jun 12, 2019 | Becton Dickinson & Company BD Vacutainer Lithium HeparinN 75 USP Units Blood Collection Tubes, Catalog Number 367884 Terminated |
JKA | None listed |
| Jun 12, 2019 | Becton Dickinson & Company BD Vacutainer LH (Lithium Heparin) 68 I.U. Plus Blood Collection Tubes, Catalog Number 368884 Terminated |
JKA | None listed |
| Jun 12, 2019 | Becton Dickinson & Company BD Vacutainer LH (Lithium Heparin) 102 I.U. Plus Blood Collection Tubes, Catalog Number 368886 Terminated |
JKA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.