510(k) K855089 ยท DQX Wire, Guide, Catheter
PERCUTANEOUS GUIDEWIRE PLACEMENT SYRINGE 50505
| Applicant | Dlp, Inc., Grand Rapids MI, US |
| Decision | Substantially Equivalent, Feb 18, 1986 |
| Received | Dec 20, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K855089
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.