510(k) K780896 ยท GCB Needle, Catheter
NEEDLES, DESIGN CHANGE, IV CATHETERS
| Applicant | Jelco Laboratories KS, US |
| Decision | Substantially Equivalent, Aug 23, 1978 |
| Received | May 30, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780896
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.