510(k) K183148 ยท GEI Electrosurgical, Cutting & Coagulation & Accessories
OKLand Patient Return Electrode Pad
| Applicant | Auckland Medical Polymer(Tianjin) Co., Ltd., Tianjin, CN |
| Decision | Substantially Equivalent, Feb 4, 2020 |
| Received | Nov 13, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K183148
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.