510(k) K892885 ยท BTL Ventilator, Emergency, Powered (Resuscitator)
RESUBMITTED RD1000 NEOPUFF INFANT RESUSCITATOR
| Applicant | Fisher & Paykel Electronics , Ltd., Auckland, New Zealand, NZ |
| Decision | Substantially Equivalent, Oct 6, 1989 |
| Received | Apr 19, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892885
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.