510(k) K072021 ยท BTM Ventilator, Emergency, Manual (Resuscitator)
NEOPIP INFANT RESUSCITATOR
| Applicant | Neoforce Group, Inc., Ivyland PA, US |
| Decision | Substantially Equivalent, Sep 12, 2007 |
| Received | Jul 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072021
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.