510(k) K133751 ยท JIT Calibrator, Secondary
DIAMOND DIAGNOSTICS ISE SERUM STANDARDS, DIAMOND DIAGNOSTICS ISE URINE STANDARDS
| Applicant | Diamond Diagnostics, Inc., Holliston MA, US |
| Decision | Substantially Equivalent, Aug 8, 2014 |
| Received | Dec 9, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133751
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.