510(k) K880705 ยท DKB Calibrators, Drug Mixture
THERAPEUTIC DRUG STANDARD
| Applicant | Verichem Laboratories, Inc., East Providence RI, US |
| Decision | Substantially Equivalent, May 31, 1988 |
| Received | Feb 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880705
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.