510(k) K760724 ยท EKX Handpiece, Direct Drive, Ac-Powered
PERITONEAL DIALYSIS SYSTEM
| Applicant | Physio-Control Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 23, 1976 |
| Received | Sep 27, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760724
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.