510(k) K920332 ยท CAF Nebulizer (Direct Patient Interface)
HEART NUBULIZER
| Applicant | Vortran Medical Technology 1, Inc., Sacramento CA, US |
| Decision | Substantially Equivalent, May 26, 1992 |
| Received | Jan 23, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920332
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.