510(k) K132325 ยท NPK Barrier, Synthetic, Intraoral
GUIDOR BIORESORBABLE MATRIX BARRIER
| Applicant | Sunstar Americas, Inc., New York NY, US |
| Decision | Substantially Equivalent, Oct 29, 2013 |
| Received | Jul 26, 2013 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K132325
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.