510(k) K921463 ยท ESD Hearing Aid, Air-Conduction, Prescription
PHILIPS 31 SERIES IN THE EAR HEARING AID
| Applicant | Philips Hearing Instruments Co., Mahwah NJ, US |
| Decision | Substantially Equivalent, May 22, 1992 |
| Received | Mar 27, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921463
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.