510(k) K060347 ยท EKR Plugger, Root Canal, Endodontic
B&L L-BETA, MODEL WL-B1
| Applicant | B&L Biotech Co., Ltd., Deer Field IL, US |
| Decision | Substantially Equivalent, Jun 5, 2006 |
| Received | Feb 10, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060347
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.