510(k) K103421 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
ARSTASIS DILATOR ADAPTER
| Applicant | Arstasis, Inc., San Carlos CA, US |
| Decision | Substantially Equivalent, May 24, 2011 |
| Received | Nov 22, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103421
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.