510(k) K070749 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
ESTECH PERCUTANEOUS INSERTION DILATOR KIT
| Applicant | Coombs Medical Device Consulting, Alameda CA, US |
| Decision | Substantially Equivalent, Oct 24, 2007 |
| Received | Mar 19, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070749
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.