510(k) K870723 ยท ESD Hearing Aid, Air-Conduction, Prescription
HEARTECH HFX, HEARING AID
| Applicant | Hearing Tech, Inc., Minnetonka MN, US |
| Decision | Substantially Equivalent, Mar 20, 1987 |
| Received | Feb 24, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870723
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.