510(k) K890228 ยท GDF Guide, Needle, Surgical
SURGICAL NEEDLE GUIDE
| Applicant | Kinetic Medical Products, Erie PA, US |
| Decision | Substantially Equivalent, Jan 27, 1989 |
| Received | Jan 18, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890228
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.