510(k) K913367 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
MODELS MR410 & MR480 RESPIRATORY HUMIDIFIER/ACCESS
| Applicant | Fisher & Paykel Electronics , Ltd., Auckland, New Zealand, NZ |
| Decision | Substantially Equivalent, Jun 25, 1992 |
| Received | Jul 24, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913367
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.