510(k) K904755 ยท LZI Device, Assistive Listening
ACOUSTIQ LISTENING DEVICE
| Applicant | Krueger Laboratories, Tempe AZ, US |
| Decision | Substantially Equivalent, Jan 29, 1991 |
| Received | Oct 19, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904755
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.