510(k) K013360 ยท FGI Catheter, Urethrographic, Male
DFINER UROLOGICAL CATHETER
| Applicant | Neoseed Technology,Llc, Newburyport MA, US |
| Decision | Substantially Equivalent, Feb 20, 2002 |
| Received | Oct 10, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013360
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.