510(k) K191740 · HBL Holder, Head, Neurosurgical (Skull Clamp)
DORO LUCENT® iXI and iMRI Headrest System
| Applicant | Pro Med Instruments GmbH, Freiburg, DE |
| Decision | Substantially Equivalent, Feb 21, 2020 |
| Received | Jul 1, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191740
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.