510(k) K890109 ยท JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
SAFEPETTE DISPENSER
| Applicant | Safe-Tec Clinical Products, Inc., Ivyland PA, US |
| Decision | Substantially Equivalent, Feb 23, 1989 |
| Received | Jan 10, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890109
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.