510(k) K090307 ยท CAF Nebulizer (Direct Patient Interface)
DDI ULTRASONIC NEBULIZER SYSTEM
| Applicant | Diagnostic Devices, Inc., Crofton MD, US |
| Decision | Substantially Equivalent, Jun 18, 2009 |
| Received | Feb 6, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090307
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.