510(k) K933700 ยท DQO Catheter, Intravascular, Diagnostic
DYE MANAGEMENT SYSTEM
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Nov 3, 1993 |
| Received | Jul 29, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933700
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 15, 2005 | Hospira Inc. Angiographic Syringe, 10 cc Thumb Ring with Rotator Reservoir. Terminated |
DQO | None listed |
| Mar 15, 2005 | Hospira Inc. Angiographic Syringe, 12 cc Thumb Ring with Rotator Reservoir. Terminated |
DQO | None listed |
| Mar 15, 2005 | Hospira Inc. Angiographic Syringe, 12 cc Thumb Ring with Rotator Non-Reservoir. Terminated |
DQO | None listed |
| Mar 15, 2005 | Hospira Inc. Angiographic Syringe, 12 cc Palm Pad with Rotator Reservoir. Terminated |
DQO | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.