510(k) K983768 ยท IZD Probe, Uptake, Nuclear
MODIFICATION TO GAMMA GUIDANCE SYSTEM
| Applicant | Radiation Monitoring Devices, Inc., Watertown MA, US |
| Decision | Substantially Equivalent, Jul 2, 1999 |
| Received | Oct 26, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983768
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.