510(k) K943670 ยท ESD Hearing Aid, Air-Conduction, Prescription
MO6 SERIES
| Applicant | Philips Hearing Instruments Co., Mahwah NJ, US |
| Decision | Substantially Equivalent, Aug 18, 1994 |
| Received | Jul 26, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943670
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.