510(k) K110157 ยท FIE Needle, Fistula
SYSLOC MINI V3
| Applicant | JMS North America Corporation, Crofton MD, US |
| Decision | Substantially Equivalent, Feb 11, 2011 |
| Received | Jan 19, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K110157
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.