510(k) K020281 ยท NHK Resuscitator, Manual, Non Self-Inflating
MODIFICATION TO VENTLAB HYPERINFLATION BAG SYSTEM
| Applicant | Ventlab Corp., Mocksville NC, US |
| Decision | Substantially Equivalent, Feb 11, 2002 |
| Received | Jan 28, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020281
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.