510(k) K884970 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
PINSET
| Applicant | Safety Diagnostics, Inc., Waukegan IL, US |
| Decision | Substantially Equivalent, Sep 7, 1989 |
| Received | Nov 30, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884970
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.