510(k) K935757 ยท LBB Dynamometer, Ac-Powered
GREENLEAF EVAL SYSTEM/ GREENLEAF SOLOSYSTEM
| Applicant | Greenleaf Medical Systems, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Apr 15, 1994 |
| Received | Nov 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935757
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.