510(k) K073353 ยท EFB Handpiece, Air-Powered, Dental
DO-ALL DENTAL HANDPIECE LUBRICANT
| Applicant | Prodrive Systems, Inc., Ogdensburg NY, US |
| Decision | Substantially Equivalent, Dec 7, 2007 |
| Received | Nov 29, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073353
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.