510(k) K071878 ยท GZJ Stimulator, Nerve, Transcutaneous, For Pain Relief
DELTA SCANNER, DELTA SCANNER PRO, DS SPINE PRO, DS SPORTS PRO AND DS REHAB
| Applicant | Med-Lectric Corporation, Kemah TX, US |
| Decision | Substantially Equivalent, Dec 7, 2007 |
| Received | Jul 6, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071878
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.