510(k) K881970 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
MODEL MR2000 HEATED RESPIRATORY HUMIDIFIER
| Applicant | Fisher & Paykel Healthcare, Ltd., Auckland, New Zealand, NZ |
| Decision | Substantially Equivalent, Mar 9, 1989 |
| Received | May 11, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881970
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.