510(k) K170946 ยท OXO Image-Intensified Fluoroscopic X-Ray System, Mobile
Skan-C Mobile C-Arm X-Ray System - 230V Variant, Skan-C Mobile C-Arm X-Ray System - 110V Variant
| Applicant | Skanray Technologies Private Limited, Mysore, IN |
| Decision | Substantially Equivalent, Nov 24, 2017 |
| Received | Mar 30, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170946
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.