510(k) K961726 ยท DLJ Calibrators, Drug Specific
ABUSCREEN ONLINE CANNABINOIDS CALIBRATION PACK 20
| Applicant | Roche Diagnostic Systems, Inc., Branchburg NJ, US |
| Decision | Substantially Equivalent, Jul 11, 1996 |
| Received | May 3, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961726
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.