510(k) K030869 ยท KZM Device, Muscle Monitoring
BITESTRIP
| Applicant | S.L.P. , Ltd., Tel-Aviv, IL |
| Decision | Substantially Equivalent, May 14, 2004 |
| Received | Mar 19, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030869
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.