510(k) K092384 ยท MVL Cord, Retraction
LIQUICORD
| Applicant | Centrix, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Nov 4, 2009 |
| Received | Aug 5, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092384
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.