510(k) K120349 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
SONIXGPS VASCULAR ACCESS NEEDLE KIT
| Applicant | Ultrasonix Medical Corpation, Richmond, CA |
| Decision | Substantially Equivalent, Apr 9, 2012 |
| Received | Feb 6, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120349
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.