510(k) K090156 ยท FMI Needle, Hypodermic, Single Lumen
ISOLYSER SHARPS ROOM SYSTEM, MODEL 800; ISOLYSER SHARPS MANAGEMENT SYSTEM, MODELS 2400, 4000, 10000
| Applicant | Wcm Waste & Compliance Management, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Sep 1, 2009 |
| Received | Jan 22, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090156
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.