510(k) K920134 ยท ESD Hearing Aid, Air-Conduction, Prescription
PHILIPS 41 SERIES RAINBOW
| Applicant | Philips Int'L B.V., Mahwah NJ, US |
| Decision | Substantially Equivalent, Jan 24, 1992 |
| Received | Jan 13, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920134
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.