510(k) K960357 ยท JHI Visual, Pregnancy Hcg, Prescription Use
DSL ACTIVE I-HCG IRMA
| Applicant | Diagnostic Systems Laboratories, Inc., Webster TX, US |
| Decision | Substantially Equivalent, May 7, 1996 |
| Received | Jan 25, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960357
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.