510(k) K900735 ยท FMZ Incubator, Neonatal
MODEL 130 AUTOMATIC HEIGHT ADJUST (AHA) INCUBATOR
| Applicant | Preemicare Corp., Houston TX, US |
| Decision | Substantially Equivalent, May 2, 1990 |
| Received | Feb 16, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900735
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.