510(k) K890549 ยท JHI Visual, Pregnancy Hcg, Prescription Use
VENTREX COATED TUBE HCG
| Applicant | Ventrex Laboratories, Inc., Portland ME, US |
| Decision | Substantially Equivalent, Mar 28, 1989 |
| Received | Feb 3, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890549
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.