510(k) K813317 ยท NHK Resuscitator, Manual, Non Self-Inflating
DISP. HYPERINFLATION BAG SYSTEM
| Applicant | Intec Medical, Inc., Blue Springs MO, US |
| Decision | Substantially Equivalent, Mar 12, 1982 |
| Received | Nov 24, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813317
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.