510(k) K840017 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
VERTEX PERCUTANEOUS CATHETER INTRODUC
| Applicant | Professional Medical Services, Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 4, 1984 |
| Received | Jan 4, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K840017
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.