510(k) K863090 ยท GDF Guide, Needle, Surgical
PERCU GUIDE I (LOOP TYPE)
| Applicant | E-Z-Em, Inc., Westbury NY, US |
| Decision | Substantially Equivalent, Aug 29, 1986 |
| Received | Aug 13, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K863090
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.