510(k) K101551 ยท EFB Handpiece, Air-Powered, Dental
PACEMAKER HIGH-SPEED HANDPIECE MODEL PM-MQ, PM-M
| Applicant | Delma Medical Instrument (Guangzhou) Co., Ltd., Dover DE, US |
| Decision | Substantially Equivalent, Sep 9, 2010 |
| Received | Jun 4, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101551
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.