510(k) K820119 ยท KPW Device, Beam Limiting, X-Ray, Diagnostic
PODIOSCOPE BY ARROW
| Applicant | Arrow X-Ray Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 18, 1982 |
| Received | Jan 18, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K820119
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.