510(k) K862288 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
MODIFICATION OF TISSUE DILATOR
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Aug 19, 1986 |
| Received | Jun 16, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862288
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.