510(k) K860472 ยท IWE Monitor, Patient Position, Light-Beam
NUCLEAR LASER ALIGNMENT SYSTEM FOR CARDIC STRESS
| Applicant | Nuclear Diagnostics, Inc., Springfield MO, US |
| Decision | Substantially Equivalent, Jul 3, 1986 |
| Received | Feb 6, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860472
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.