510(k) K963917 ยท CAF Nebulizer (Direct Patient Interface)
HOLDEN-WALKER HUMIDIFIER-NEBULIZER KIT
| Applicant | Holden Walker Corp., Naples FL, US |
| Decision | Unknown, Feb 25, 1997 |
| Received | Sep 30, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963917
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.