510(k) K091111 ยท CAF Nebulizer (Direct Patient Interface)
RTC METERED DOSE INHALER ADAPTERS-SINGLE PATIENT USE, MODEL RTC 24-V, RTC MDI ADAPTER KIT-SINGLE PATIENT USE, MODEL RTC
| Applicant | Instrumentation Industries, Inc., Bethel Park PA, US |
| Decision | Substantially Equivalent, Dec 2, 2009 |
| Received | Apr 17, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091111
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.