510(k) K960321 ยท DPS Electrocardiograph
CARDIOCATH CATHETERIZATION LAB SYSTEM
| Applicant | Prucka Engineering, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Aug 21, 1996 |
| Received | Jan 22, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960321
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.