510(k) K894612 ยท NHK Resuscitator, Manual, Non Self-Inflating
INTERTECH NEWBORN HYPERINFLATION BAG SYSTEM
| Applicant | Intertech Resources, Inc., Fort Myers FL, US |
| Decision | Substantially Equivalent, Sep 8, 1989 |
| Received | Jul 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K894612
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.