510(k) K880925 ยท GXI Probe, Radiofrequency Lesion
DISPOSABLE WET FIELD ERASER
| Applicant | Advanced Surgical Products, Inc., Chesterfield MO, US |
| Decision | Substantially Equivalent, Apr 13, 1988 |
| Received | Mar 4, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880925
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.