510(k) K122832 ยท DRC Trocar
MOBICATH TRANSSEPTAL NEEDLE
| Applicant | Great Batch Medical, Plymouth MN, US |
| Decision | Substantially Equivalent, Dec 19, 2012 |
| Received | Sep 17, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122832
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.