510(k) K083684 ยท KNT Tubes, Gastrointestinal (And Accessories)
ENDO VIVE STANDARD REPLACEMENT GASTROSTOMY TUBE, MODEL 82XX
| Applicant | Manufacturing & Research, Inc., Tucson AZ, US |
| Decision | Substantially Equivalent, Feb 5, 2009 |
| Received | Dec 12, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083684
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.