510(k) K030855 ยท KNT Tubes, Gastrointestinal (And Accessories)
MODIFICATION TO ENDOVIVE INITIAL PLACEMENT PEG KIT, DIRECT PEJ KIT, PEG SAFETY KIT
| Applicant | Boston Scientific Corp, Natick, MA, US |
| Decision | Unknown, Apr 17, 2003 |
| Received | Mar 18, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030855
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 17, 2008 | Boston Scientific Corporation EndoVive Safety PEG Kits 24 F
Universal Product Number (UPN): MOO56648 1
The product provides nutrition directly into the stomach of adult and pediatric patients who are unable to consume by conventi Terminated |
KNT | None listed |
| Sep 17, 2008 | Boston Scientific Corporation EndoVive Safety PEG Kits 20 F
Universal Product Number (UPN): MOO566460
The product provides nutrition directly into the stomach of adult and pediatric patients who are unable to consume by conventio Terminated |
KNT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.