510(k) K914061 ยท KQX Goniometer, Ac-Powered
NK RANGE OF MOTION SENSOR, MODEL RM002
| Applicant | Nk Biotechnical Engineering Co., Minneapolis MN, US |
| Decision | Substantially Equivalent, Dec 9, 1991 |
| Received | Sep 10, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K914061
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.