510(k) K832301 ยท JCX Apparatus, Suction, Ward Use, Portable, Ac-Powered
DIRECT BONDED BRACKET REMOVER
| Applicant | Northwest Orthopedics, Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 31, 1983 |
| Received | Jul 13, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832301
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.