510(k) K861050 ยท GDF Guide, Needle, Surgical
BIOPSY ADAPTER H4222W
| Applicant | General Electric Co., Milwaukee WI, US |
| Decision | Substantially Equivalent, Apr 2, 1986 |
| Received | Mar 19, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K861050
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.