510(k) K831242 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
LITHIUM HEPARINIZED BLOOD COLLECT-TUBE
| Applicant | American Dade, Mchenry IL, US |
| Decision | Substantially Equivalent, May 16, 1983 |
| Received | Apr 15, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K831242
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.