510(k) K880981 ยท IWE Monitor, Patient Position, Light-Beam
A2J MZ 44 B TYPE
| Applicant | A2j, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Apr 22, 1988 |
| Received | Mar 8, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880981
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.