510(k) K914419 ยท HIO Sampler, Amniotic Fluid (Amniocentesis Tray)
AMNIOTEST(TM)
| Applicant | Pro-Lab, Inc., Ontario Canada M5m 1c9, CA |
| Decision | Substantially Equivalent, Sep 1, 1993 |
| Received | Oct 3, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914419
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.