510(k) K190118 ยท GXY Electrode, Cutaneous
Dr-Ho's Foot Pad Electrode (Models: DHFRE-I, CP-I, CP-II, CP-III)
| Applicant | Guangzhou Xinbo Electronic Co., Ltd., Panyu, CN |
| Decision | Substantially Equivalent, May 13, 2020 |
| Received | Jan 24, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190118
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.