510(k) K081550 ยท ELC Scaler, Ultrasonic
BONART ULTRASONIC SCALER, MOEDLS ART-P3II PRO AND ART-MII PRO
| Applicant | Bonart Co., Ltd., Walnut CA, US |
| Decision | Substantially Equivalent, Aug 28, 2008 |
| Received | Jun 3, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081550
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.