510(k) K191846 ยท HQB Photocoagulator And Accessories
MAXReach Laser Probe
| Applicant | Vortex Surgical, Inc., Chesterfield MO, US |
| Decision | Substantially Equivalent, Dec 23, 2019 |
| Received | Jul 10, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191846
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.