510(k) K812332 ยท KPR System, X-Ray, Stationary
KERMATH L/C ARM
| Applicant | Kermath Mfg. Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 16, 1981 |
| Received | Aug 18, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812332
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.