510(k) K780732 ยท DLJ Calibrators, Drug Specific
PROCAINAMIDE CALIBRATOR KIT
| Applicant | Vitek Systems, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Nov 22, 1978 |
| Received | May 2, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780732
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.