510(k) K030146 ยท NVK Laser, Dental, Soft Tissue
KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+
| Applicant | Kavo America, Lake Zurich IL, US |
| Decision | Substantially Equivalent, Aug 3, 2005 |
| Received | Jan 15, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K030146
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.