510(k) K073706 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
RESPIRATORY HUMIDIFIER, MODEL MR850
| Applicant | Fisher & Paykel Healthcare, Ltd., East Tamaki, Auckland, NZ |
| Decision | Substantially Equivalent, Mar 31, 2008 |
| Received | Dec 31, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073706
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.