510(k) K943929 ยท KQX Goniometer, Ac-Powered
DATAGLOVE AND MOVEMENT ANALYSIS SYSTEM (MAS)
| Applicant | Greenleaf Medical Systems, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, May 15, 1995 |
| Received | Aug 12, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943929
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.