510(k) K962319 ยท IZD Probe, Uptake, Nuclear
NEOPROBE 1000 GEN 1C PORTABLE RADIOISOTOPE DETECTOR & ACCESSORIES
| Applicant | Neoprobe Corp., Dublin OH, US |
| Decision | Substantially Equivalent, Sep 13, 1996 |
| Received | Jun 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962319
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.