510(k) K882804 ยท DQX Wire, Guide, Catheter
0.014 PERIPHERAL GUIDE WIRE
| Applicant | Intensive Technology, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Oct 28, 1988 |
| Received | Jul 7, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882804
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.