510(k) K971622 ยท KIF Resin, Root Canal Filling
MAX-I-PROBE ENDODONTIC SEALER DELIVERY SYSTEM
| Applicant | Mpl Technologies, Inc., Franklin Park IL, US |
| Decision | Substantially Equivalent, Jun 20, 1997 |
| Received | May 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971622
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.