510(k) K150932 ยท DRE Dilator, Vessel, For Percutaneous Catheterization
Sheath Introducer
| Applicant | Bioteque Corp., Taipei, TW |
| Decision | Substantially Equivalent, Jul 22, 2016 |
| Received | Apr 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150932
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.