510(k) K884723 ยท KQX Goniometer, Ac-Powered
(DATAGLOVE) HAND IMPAIRMENT EVALUATION SYSTEM
| Applicant | Greenleaf Medical Systems, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Feb 8, 1989 |
| Received | Nov 10, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884723
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.