510(k) K061200 ยท BZD Ventilator, Non-Continuous (Respirator)
PRESTIGE CPAP FLOW GENERATOR WITH PRESTIGE HUMIDIFIER
| Applicant | Resmed, Ltd., Poway CA, US |
| Decision | Substantially Equivalent, Jul 20, 2006 |
| Received | May 1, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061200
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.