510(k) K781019 ยท KKY Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction
SURG. GOWN & DRAPE, LOW LINT TREATMENT
| Applicant | Kimberly-Clark Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 14, 1978 |
| Received | Jan 16, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781019
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.