510(k) K912724 ยท NPK Barrier, Synthetic, Intraoral
GUIDOR(TM)
| Applicant | Procordia Oratech AB, Huddinge, Sweden, SE |
| Decision | Substantially Equivalent for Some Indications, May 13, 1993 |
| Received | Jun 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912724
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.