510(k) K873930 ยท CAF Nebulizer (Direct Patient Interface)
AEROSOL DELIVERY SYSTEM (AERO-TECH II)
| Applicant | Cadema Medical Products, Inc., Middletown NY, US |
| Decision | Substantially Equivalent, Dec 7, 1987 |
| Received | Sep 25, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873930
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.