510(k) K093312 ยท KGC Tube, Gastro-Enterostomy
KIMBERLY-CLARK GASTROINTESTINAL ANCHOR SET WITH SAF-T-PEXY FASTENERS, ENTERNAL ACCESS DILATION SYSTEM
| Applicant | Kimberly-Clark Corp., Roswell GA, US |
| Decision | Substantially Equivalent, Dec 8, 2009 |
| Received | Oct 22, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K093312
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.