510(k) K111644 ยท DRC Trocar
MOBICATH TRANSSEPTAL NEEDLE
| Applicant | Great Batch Medical, Plymouth MN, US |
| Decision | Substantially Equivalent, Oct 3, 2011 |
| Received | Jun 13, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111644
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.