510(k) K972433 ยท DLJ Calibrators, Drug Specific
CEDIA DIGOXIN CALIBRATORS
| Applicant | Boehringer Mannheim Corp., Concord CA, US |
| Decision | Substantially Equivalent, Jul 24, 1997 |
| Received | Jun 30, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972433
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.