510(k) K853282 ยท EID Syringe, Restorative And Impression Material
CENTRIX RIBBON TUBES
| Applicant | Centrix, Inc., Stratford CT, US |
| Decision | Substantially Equivalent, Aug 23, 1985 |
| Received | Aug 5, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K853282
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.