510(k) K954041 ยท FMI Needle, Hypodermic, Single Lumen
G.R.E.E.N. DISPOSAL CONTAINER (NOTE: G.R.E.E.N. IS AN ACRONYM FOR GLAXO RETRIEVAL EFFORT FOR EXPENDED NEEDLES)
| Applicant | Glaxo, Inc., Research Triangle Park NC, US |
| Decision | Substantially Equivalent, Oct 16, 1995 |
| Received | Aug 29, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954041
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.