510(k) K172512 ยท LCX Kit, Test, Pregnancy, Hcg, Over The Counter
ACRO HCG Pregnancy Rapid Test
| Applicant | Acro Biotech, Inc., Rancho Cucamonga CA, US |
| Decision | Substantially Equivalent, Feb 2, 2018 |
| Received | Aug 21, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K172512
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.