510(k) K022681 ยท DHA System, Test, Human Chorionic Gonadotropin
AZOG, INC. HCG ONE-STEP URINE PREGNANCY TEST (DEVICE OR CASSETTE)
| Applicant | Azog, Inc., Phillipsburg NJ, US |
| Decision | Substantially Equivalent, Nov 1, 2002 |
| Received | Aug 12, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022681
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.