510(k) K952200 ยท KDG Chisel (Osteotome)
OMNI-JUG
| Applicant | Waterstone Medical, Inc., Bethesda MD, US |
| Decision | Substantially Equivalent, Jun 29, 1995 |
| Received | May 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952200
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.