510(k) K885138 ยท GIO Tube, Collection, Capillary Blood
CAPILLARY TUBE, BLOOD COLLECTION
| Applicant | Coeur Laboratories, Inc., Raleigh NC, US |
| Decision | Substantially Equivalent, Feb 7, 1989 |
| Received | Dec 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885138
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.