510(k) K880411 ยท CAF Nebulizer (Direct Patient Interface)
DEY-VIAL SODIUM CHLORIDE SOLUTION, USP, STERILE
| Applicant | Dey Laboratories, Inc., Concord CA, US |
| Decision | Substantially Equivalent, Feb 29, 1988 |
| Received | Feb 1, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880411
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.