510(k) K905548 ยท DQX Wire, Guide, Catheter
PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY GUIDEWIRE
| Applicant | Mallinckrodt Medical, St Louis MO, US |
| Decision | Substantially Equivalent, Feb 25, 1991 |
| Received | Dec 11, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K905548
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.