510(k) K884623 ยท GIO Tube, Collection, Capillary Blood
SAFE-TEC CAPILLARY BLOOD COLLECTION TUBE
| Applicant | Safe-Tec Clinical Products, Inc., Ivyland PA, US |
| Decision | Substantially Equivalent, Dec 1, 1988 |
| Received | Nov 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884623
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.