510(k) K904127 ยท IWE Monitor, Patient Position, Light-Beam
A2J TELEMETER
| Applicant | A2j, Inc., Fredericksburg VA, US |
| Decision | Substantially Equivalent, Jan 4, 1991 |
| Received | Aug 29, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904127
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.