510(k) K013511 ยท FSW Light, Surgical, Endoscopic
XENALIGHT MODELS # AX9125 (100-120V~); # AX9225 (220-240V~)
| Applicant | Aculux, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Feb 1, 2002 |
| Received | Oct 22, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013511
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.