510(k) K102649 ยท BTM Ventilator, Emergency, Manual (Resuscitator)
NEOPOP INFANT RESUSCITATOR WITH FLOW METER
| Applicant | Neoforce Group, Inc., Ivyland PA, US |
| Decision | Substantially Equivalent, Jan 6, 2011 |
| Received | Sep 14, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102649
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.