ECHOSINE 1000, PULSED A-MODE ULTRASOUND DEVICE
| Applicant | American Electromedics Corp., Hudson NH, US |
| Decision | Substantially Equivalent, Mar 22, 1983 |
| Received | Dec 10, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K837029
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.