510(k) K232805 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Kronos Electrocautery Device
| Applicant | Single Pass, Inc., Lake Forest CA, US |
| Decision | Substantially Equivalent, Apr 25, 2024 |
| Received | Sep 12, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232805
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.