510(k) K922550 ยท KQX Goniometer, Ac-Powered
ROMAS (RANGE OF MOTION ASSESSMENT SYSTEM)
| Applicant | Verimed Holdings, Inc., Fort Lauderdale FL, US |
| Decision | Substantially Equivalent, Dec 10, 1992 |
| Received | May 29, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922550
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.