510(k) K163037 ยท HRX Arthroscope
Intra medullary endo-transilluminating device (iMET device)
| Applicant | WeMED Bio-Tech, Inc., Taipei City, TW |
| Decision | Substantially Equivalent, Feb 17, 2017 |
| Received | Oct 31, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163037
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.