510(k) K013308 ยท NHK Resuscitator, Manual, Non Self-Inflating
VENTLAB HYPERINFLATION BAG SYSTEM
| Applicant | Ventlab Corp., Mocksville NC, US |
| Decision | Substantially Equivalent, Dec 20, 2001 |
| Received | Oct 4, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013308
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.