510(k) K960229 ยท ETW Calibrator, Hearing Aid / Earphone And Analysis Systems
RESOUND REAL EAR LOUDNESS MAPPING (RELM) SYSTEM
| Applicant | Resound Corp., Redwood City CA, US |
| Decision | Substantially Equivalent, Mar 7, 1996 |
| Received | Jan 17, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960229
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.