510(k) K112231 ยท GXI Probe, Radiofrequency Lesion
LCCS INSULATED SPINAL NEEDLE (RF CANNULA)
| Applicant | Lccs Products Limited, Shenzhen, Guangdong, CN |
| Decision | Substantially Equivalent, Aug 19, 2011 |
| Received | Aug 4, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112231
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.