510(k) K013843 ยท BZD Ventilator, Non-Continuous (Respirator)
AUTOSET SPIRIT CPAP SYSTEM
| Applicant | Resmed Corp, Poway CA, US |
| Decision | Substantially Equivalent, Jul 16, 2002 |
| Received | Nov 20, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013843
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.