510(k) K991932 ยท FPA Set, Administration, Intravascular
INTRAVASCULAR ADMINISTRATION SET
| Applicant | The Kipp Group, Ontario CA, US |
| Decision | Substantially Equivalent, Aug 20, 1999 |
| Received | Jun 8, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K991932
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 27, 2003 | Abbott Laboratories HPD/ADD I.V. Extension Sets; sterile, Rx, single use devices; Abbott Laboratories, North Chicago, IL 60064 USA; 22 different sets listed in the code information section below. Please Note: items p, q & r (li Terminated |
FPA | None listed |
| Jun 5, 2003 | Abbott Laboratories HPD/ADD LifeShield Latex-Free 150 mL Burette Set, Nonvented, 117 Inch with Prepierced Injection Site, Backcheck Valve, 2 CLAVE Ports and Removable 4-Way High Flow Stopcock Microdrip Soluset; Product 19292; Ma Terminated |
FPA | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.