510(k) K173229 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
Preview Digital Pregnancy Test
| Applicant | Guangzhou Wondfo Biotech Co., Ltd., Guangzhou, CN |
| Decision | Substantially Equivalent, Mar 12, 2018 |
| Received | Oct 4, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173229
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.