510(k) K800003 ยท GLE Mixer, Blood Tube
CORTEX DOUBLE HELIX SAMPLER
| Applicant | Cortex Research Corp., Walker MI, US |
| Decision | Substantially Equivalent, Feb 1, 1980 |
| Received | Jan 2, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800003
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.