510(k) K060222 ยท NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter
LOW BACK PAIN RELIEF SYSTEM /MODELS GM310PP,GM320PP,GM321PP, AND GM330PP
| Applicant | Gemore Technology Co, Ltd., Tan Shui, New Taipei City, TW |
| Decision | Substantially Equivalent, Apr 28, 2006 |
| Received | Jan 30, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060222
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.