510(k) K893873 ยท DHA System, Test, Human Chorionic Gonadotropin
SINGLE AND DUAL BAND DIPSTICK HCG TEST
| Applicant | Ampcor, Inc., Bridgeport NJ, US |
| Decision | Substantially Equivalent, Aug 21, 1989 |
| Received | May 26, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893873
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.