510(k) K222284 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Voyant Maryland Fusion device with Single-Step Activation (EB212, EB213, EB214)
| Applicant | Applied Medical Resources Corporation, Rancho Santa CA, US |
| Decision | Substantially Equivalent, Oct 14, 2022 |
| Received | Aug 1, 2022 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K222284
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.