510(k) K190804 ยท HRX Arthroscope
HydroCision TenJet Device
| Applicant | Hydrocision, Inc., North Billerica MA, US |
| Decision | Substantially Equivalent, Jun 5, 2019 |
| Received | Mar 29, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K190804
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.