510(k) K770183 ยท FPB Filter, Infusion Line
O.22/UM FILTERSET W/FLASHBACK
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Feb 9, 1977 |
| Received | Jan 27, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770183
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 15, 2010 | Hospira Inc. Latex-free, Primary I.V. Set, vented, 73 inch with flashback bulb, 15 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica, list 8962-48. Terminated |
FPA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.