510(k) K051487 ยท KHJ Polymer, Ent Synthetic-Polyamide (Mesh Or Foil Material)
DRG LARYNGEAL AUGMENTATION IMPLANT DEVICE
| Applicant | Doctor'S Research Group, Inc., Plymouth CT, US |
| Decision | Substantially Equivalent, Dec 22, 2005 |
| Received | Jun 6, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051487
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.