510(k) K924447 ยท KZF Device, Medical Examination, Ac Powered
VITAPEN
| Applicant | Vitajet Corp., Laguna Hills CA, US |
| Decision | Substantially Equivalent, Sep 27, 1993 |
| Received | Sep 1, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K924447
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.