510(k) K151877 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
MicroTract Access System
| Applicant | Arstasis, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Aug 7, 2015 |
| Received | Jul 9, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151877
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.