510(k) K881701 ยท IYB Tube Mount, X-Ray, Diagnostic
RADKOR SFC-21
| Applicant | Radkor, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Sep 8, 1988 |
| Received | Apr 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881701
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.