510(k) K921725 ยท ESD Hearing Aid, Air-Conduction, Prescription
PHILIP XP SERIES, IN-THE CANAL HEARING AID
| Applicant | Philips Hearing Instruments Co., Mahwah NJ, US |
| Decision | Substantially Equivalent, Aug 11, 1992 |
| Received | Apr 9, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921725
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.