510(k) K022648 ยท KNT Tubes, Gastrointestinal (And Accessories)
ENDOVIVE INITIAL PLACEMENT DIRECT PEJ KIT, MODELS 6520 & 6521
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Sep 5, 2002 |
| Received | Aug 9, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022648
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.