510(k) K142309 ยท MVR Device, Anastomotic, Microvascular
GEM Flow COUPLER Device and System
| Applicant | Synovis Life Technologies, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Sep 16, 2014 |
| Received | Aug 19, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K142309
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.