510(k) K053203 ยท CAF Nebulizer (Direct Patient Interface)
MYNEB NEBULIZER, MODEL RDD100
| Applicant | Respironics New Jersey, Inc., Cedar Grove NJ, US |
| Decision | Substantially Equivalent, Dec 20, 2005 |
| Received | Nov 16, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K053203
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.