510(k) K933850 ยท ESD Hearing Aid, Air-Conduction, Prescription
PHILIPS 45 SERIES
| Applicant | Philips Hearing Instruments Co., Mahwah NJ, US |
| Decision | Substantially Equivalent, Sep 7, 1993 |
| Received | Aug 6, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K933850
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.