510(k) K022241 ยท NHI Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief
VERTIS PNT CONTROL UNIT, MODEL CU 100; VERTIS PNT SAFEGUIDE-CERVICAL, MODEL SG 102-XXX
| Applicant | Vertis Neuroscience, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Sep 11, 2002 |
| Received | Jul 11, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022241
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.