510(k) K060032 ยท GZI Stimulator, Neuromuscular, External Functional
RT300-S, MODEL FA100052; RT300-SP, MODEL FA100053
| Applicant | Restorative Therapies, Inc., Baltimore MD, US |
| Decision | Substantially Equivalent, Mar 10, 2006 |
| Received | Jan 5, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060032
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.