510(k) K951678 ยท LXB Hearing Aid, Bone Conduction
HI SONIC 2000 DIGITAL HEARING INSTRUMENT
| Applicant | Hearing Innovations, Inc., Washington, D.C. DC, US |
| Decision | Substantially Equivalent, Jun 7, 1995 |
| Received | Apr 11, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951678
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.