510(k) K001588 ยท GXI Probe, Radiofrequency Lesion
ARTHROCARE SYSTEM 2000 CONTROLLER, ARTHROCARE SYSTEM 2000 CABLE, ARTHROCARE SYSTEM 2000 FOOTSWITCH, ARTHROCARE SYSTEM 20
| Applicant | Arthrocare Corp., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Aug 17, 2000 |
| Received | May 23, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K001588
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.