510(k) K880739 ยท LXI Guide, Drill, Ligament
DYONICS DRILL GUIDE/ISOMETER SYSTEM
| Applicant | Dyonics, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Mar 21, 1988 |
| Received | Feb 24, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880739
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.