510(k) K011702 ยท NHI Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief
VERTIS PNT CONTROL UNIT, VERTIS PNT SAFEGUIDE KIDS, MODELS CU100, SGXXX
| Applicant | Vertis Neuroscience, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Dec 21, 2001 |
| Received | Jun 1, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011702
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.