510(k) K936000 ยท BTT Humidifier, Respiratory Gas, (Direct Patient Interface)
PURITAN-BENNETT CASCADE I SERIES HUMIDIFIER MODIFICATION
| Applicant | Puritan Bennett Corp., Carlsbad CA, US |
| Decision | Substantially Equivalent, Aug 15, 1994 |
| Received | Dec 15, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K936000
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.