510(k) K862923 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
MR620 DUAL SERVO HEATED ANAESTHESIA HUMIDIFIER
| Applicant | Fisher & Paykel Allied Products , Ltd., Auckland, New Zealand, NZ |
| Decision | Substantially Equivalent, Sep 23, 1986 |
| Received | Aug 1, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862923
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.