510(k) K780880 ยท KDC Instrument, Surgical, Disposable
Y-TYPE BLOOD SET
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Jun 30, 1978 |
| Received | May 30, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780880
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Apr 19, 2011 | Hospira Inc. Hospira Latex-Free Blood Secondary Set, 26 Inch with Secure Lock; a sterile Rx tubing set for the administration of fluids from a blood bag in series with an I.V. solution bottle and I.V. set; Made in Terminated |
KDC | None listed |
| Apr 19, 2011 | Hospira Inc. Hospira LifeShield Latex-Free HEMA Y-Type Blood Set, Nonvented, 100 Inch with Clave and Secure Lock; a sterile Rx tubing set for the alternate administration of fluids from a blood bag and I.V. soluti Terminated |
KDC | None listed |
| Apr 19, 2011 | Hospira Inc. Hospira LifeShield Latex-Free HEMA Y-Type Blood Set, Nonvented, 99 Inch with Drip Chamber Pump, 210 Micron Filter, Prepierced Injection Site and Secure Lock; a sterile Rx tubing set for the alternate Terminated |
KDC | None listed |
| Apr 15, 2010 | Hospira Inc. Lifeshield, latex-free, Y-Type Blood Set, nonvented, 100 inch with CLAVE and secure lock, 10 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica, list 12450- Terminated |
FPA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.