510(k) K873647 ยท GIO Tube, Collection, Capillary Blood
VENTRESCREEN CAPILLARY BLOOD COLLECTION TUBE
| Applicant | Ventrex Laboratories, Inc., Portland ME, US |
| Decision | Substantially Equivalent, Oct 20, 1987 |
| Received | Sep 9, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873647
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.