510(k) K934140 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
MR290 HUMIDIFICATION CHAMBER SINGLE USE
| Applicant | Fisher & Paykel Electronics , Ltd., Auckland, New Zealand, NZ |
| Decision | Substantially Equivalent, Jan 24, 1994 |
| Received | Aug 25, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K934140
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.