510(k) K072500 ยท DHA System, Test, Human Chorionic Gonadotropin
ONE STEP HCG URINE/SERUM TEST
| Applicant | Guangzhou Wondfo Biotech Co., Ltd., Yardley PA, US |
| Decision | Substantially Equivalent, Apr 21, 2009 |
| Received | Sep 5, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072500
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.