510(k) K072398 ยท GZI Stimulator, Neuromuscular, External Functional
RT300-S AND RT300-SP FES CYCLE ERGOMETER
| Applicant | Restorative Therapies, Inc., Baltimore MD, US |
| Decision | Substantially Equivalent, Nov 21, 2007 |
| Received | Aug 27, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072398
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.