510(k) K170183 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
Cetus system, Cetus probe
| Applicant | A.R.C Laser GmbH, Nurnberg, DE |
| Decision | Substantially Equivalent, Sep 27, 2017 |
| Received | Jan 23, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170183
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.