510(k) K182833 ยท EIH Powder, Porcelain
ArgenZ Liquid Shade, ArgenZ Incisal Effect, ArgenZ Color Modifier, ArgenZ Pontic Reducer
| Applicant | The Argen Corporation, San Diego CA, US |
| Decision | Substantially Equivalent, Feb 8, 2019 |
| Received | Oct 9, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182833
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.