510(k) K141002 ยท HRX Arthroscope
VS3 STEREOSCOPIC HIGH DEFINITION VISION SYSTEM
| Applicant | Visionsense, Ltd., Monroe CT, US |
| Decision | Substantially Equivalent, Jun 26, 2014 |
| Received | Apr 18, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141002
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.