510(k) K062758 ยท GXD Generator, Lesion, Radiofrequency
OWL URF-3AP
| Applicant | Diros Technology, Inc., Markham, Ontario, CA |
| Decision | Substantially Equivalent, Sep 27, 2006 |
| Received | Sep 15, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062758
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.