510(k) K912339 ยท ESD Hearing Aid, Air-Conduction, Prescription
PHILIPS M30 IN-THE-EAR HEARING AID
| Applicant | Philips Hearing Instruments Co., Mahwah NJ, US |
| Decision | Substantially Equivalent, Jun 7, 1991 |
| Received | May 24, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K912339
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.