510(k) K932753 ยท DKB Calibrators, Drug Mixture
ROCHE ABUSCREEN TRI-LEVEL REFERENCE CONTROLS
| Applicant | Roche Diagnostic Systems, Inc., Branchburg NJ, US |
| Decision | Substantially Equivalent, Jul 22, 1993 |
| Received | May 28, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K932753
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.