510(k) K133763 ยท FCG Biopsy Needle
SONOTIP PRO AND PRO FLEX EBUS-TBNA NEEDLE SYSTEM
| Applicant | Medi-Globe Corporation, Tempe AZ, US |
| Decision | Substantially Equivalent, May 15, 2014 |
| Received | Dec 11, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133763
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.