510(k) K911807 ยท CAF Nebulizer (Direct Patient Interface)
METERED DOSE INHALER (MDI) SPACER
| Applicant | Health Products, Inc., Cedar Grove NJ, US |
| Decision | Substantially Equivalent, Oct 23, 1991 |
| Received | Apr 23, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911807
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.