510(k) K902905 ยท DQY Catheter, Percutaneous
COOK CORONARY GUIDING CATHETER
| Applicant | Cook, Inc., Bloomington IN, US |
| Decision | Substantially Equivalent, Sep 4, 1990 |
| Received | Jul 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902905
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 22, 2016 | Cook Inc. White Lumax Guiding Coaxial Catheter
Catheter, Percutaneous
Intended for the delivery of angioplasty balloons and other types of interventional devices. Terminated |
DQY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.