510(k) K972484 ยท DQY Catheter, Percutaneous
ACS VIKING GUIDING CATHETER
| Applicant | Guidant Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Sep 26, 1997 |
| Received | Jul 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972484
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 13, 2008 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation 6F Viking Guiding Catheter, Percutaneous catheter, Shape ALR 1.2, Part Number: 1001934-06, Abbott Vascular, Santa Clara, CA 95054.
Designed to provide a pathway trough which therapeutic and diagnosti Terminated |
DQY | None listed |
| Aug 13, 2008 | Abbott Vascular-Cardiac Therapies dba Guidant Corporation 6F Viking Guiding Catheter, Percutaneous catheter Shape BP-L, Part Number: 1001970-06, Abbott Vascular, Santa Clara, CA 95054.
Intended to provide a pathway through which therapeutic and diagnostic d Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.