510(k) K091759 ยท KNT Tubes, Gastrointestinal (And Accessories)
SINGLE USE SPLINTING TUBE, MODELS ST-Y0002-S, ST-Y0002-H, ST-Y0003-S AND ST-Y0003-H
| Applicant | Olympus Medical Systems Corporation, Center Valley PA, US |
| Decision | Substantially Equivalent, Sep 18, 2009 |
| Received | Jun 16, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091759
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.