510(k) K170886 ยท CAF Nebulizer (Direct Patient Interface)
HOMED Mesh Nebulizer
| Applicant | Shenzhen Homed Medical Device Co., Ltd., Shenzhen, CN |
| Decision | Substantially Equivalent, Jun 21, 2018 |
| Received | Mar 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170886
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.