510(k) K181982 ยท HRX Arthroscope
MIDAScope and Introducer Kit, and MIDASystem
| Applicant | Intravu, Inc., Redwood City CA, US |
| Decision | Substantially Equivalent, Aug 21, 2018 |
| Received | Jul 25, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181982
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.