510(k) K020120 ยท KNT Tubes, Gastrointestinal (And Accessories)
ENDOVIVE INITIAL PLACEMENT DIRECT PEJ KIT, ENDOVIVE STANDARD PROFILE BALLOON REPLACEMENT, MODELS 6520, 6521, 6220
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Substantially Equivalent, Aug 2, 2002 |
| Received | Jan 14, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020120
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.