510(k) K951896 ยท ESD Hearing Aid, Air-Conduction, Prescription
INTELIVENIENCE PROGRAMMABLE FULL DYNAMIC RANGE COMPRESSION BEHIND THE EAR HEARING INSTRUMENT
| Applicant | Siemens Hearing Instruments, Inc., Piscataway NJ, US |
| Decision | Substantially Equivalent, May 30, 1995 |
| Received | Apr 24, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951896
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.