510(k) K951663 ยท EJJ Alloy, Amalgam
TYTIN R
| Applicant | Kerr Corporation (Danbury), Glendora CA, US |
| Decision | Substantially Equivalent, Jun 6, 1995 |
| Received | Apr 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951663
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jun 13, 2014 | Kerr Corporation Tytin Regular Set, Double Spill, 50 Capsules, Part Number 29948, Lot Number 3-1294.
The intended use of this device is to be used as a dental restorative material in the treatment of dental caries. Terminated |
EJJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.