510(k) K091380 ยท MVL Cord, Retraction
CORDCAP
| Applicant | Centrix, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, Jul 30, 2009 |
| Received | May 11, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091380
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.