510(k) K871187 ยท JIS Calibrator, Primary
LITHIUM INTERNAL STANDARD 3000 MEQ/L #60084
| Applicant | In Vitro Diagnostics, Inc., Shelton CT, US |
| Decision | Substantially Equivalent, May 28, 1987 |
| Received | Mar 24, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K871187
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.