510(k) K960854 ยท CAF Nebulizer (Direct Patient Interface)
SIEMENS SERVO ULTRA NEBULIZER 345
| Applicant | Pacesetter, Inc., North Attleboro MA, US |
| Decision | Substantially Equivalent, Dec 23, 1996 |
| Received | Mar 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960854
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.