510(k) K131117 ยท EIH Powder, Porcelain
ZIRMON SERIES
| Applicant | Kuwotech Co., Ltd., Anaheim CA, US |
| Decision | Substantially Equivalent, Jul 26, 2013 |
| Received | Apr 22, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131117
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.