510(k) K160290 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
Valleylab REM Polyhesive Infant Patient Return Electrode
| Applicant | Covidien, LLC, Boulder CO, US |
| Decision | Substantially Equivalent, May 19, 2016 |
| Received | Feb 3, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160290
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.