510(k) K212395 ยท CAF Nebulizer (Direct Patient Interface)
Nebulizer
| Applicant | Shenzhen Homed Medical Device Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Mar 25, 2022 |
| Received | Aug 2, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212395
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.