510(k) K801063 ยท DWX Stripper, Artery, Intraluminal
HALL ARTERIAL OSCILLATOR
| Applicant | American Sterilizer Co., Walker MI, US |
| Decision | Substantially Equivalent, Sep 26, 1980 |
| Received | May 6, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801063
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.