510(k) K930348 ยท FDX Endoscopic Cytology Brush
COMBO CATH WIRE-GUIDED CYTOLOGY SYSTEM
| Applicant | Boston Scientific Corp, San Jose CA, US |
| Decision | Substantially Equivalent, Sep 3, 1993 |
| Received | Jan 25, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930348
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.