510(k) K060364 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
VACU LAB PLAIN TUBE, VACU LAB GEL & CLOT ACTIVATOR TUBE, VACU LAB COAGULATION TUBE
| Applicant | Teco Diagnostics, Anaheim CA, US |
| Decision | Substantially Equivalent, Jun 15, 2006 |
| Received | Feb 13, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060364
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.