510(k) K191605 ยท PLV Dental Stereotaxic Instrument
Neocis Guidance System (NGS)
| Applicant | Neocis, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Sep 11, 2019 |
| Received | Jun 17, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191605
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.