510(k) K160423 ยท FCG Biopsy Needle
Perineologic Access Needle
| Applicant | Corbin Clinical Resources, LLC, Cumberland MD, US |
| Decision | Substantially Equivalent, Sep 2, 2016 |
| Received | Feb 16, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160423
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.