510(k) K190144 ยท LFD Saliva, Artificial
MucoPEG
| Applicant | Sunbio, Inc., Gunpo-Si, KR |
| Decision | Substantially Equivalent, Nov 5, 2019 |
| Received | Jan 29, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190144
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.