510(k) K932141 ยท DQO Catheter, Intravascular, Diagnostic
CARDIAC CATHETERIZATION KIT
| Applicant | Abbott Laboratories, Abbott Park IL, US |
| Decision | Substantially Equivalent, Sep 22, 1994 |
| Received | Apr 22, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932141
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 15, 2005 | Hospira Inc. Catheterization Kits containing Angiographic Syringes with rotator connector. Terminated |
DQO | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.