510(k) K061166 ยท NHI Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief
DEEPWAVE PERCUTANEOUS NEUROMODULATION PAIN THERAPY SYSTEM
| Applicant | Biowave Corporation, North Attleboro MA, US |
| Decision | Substantially Equivalent, Aug 15, 2006 |
| Received | Apr 27, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061166
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.