510(k) K062306 ยท GGC Control, Plasma, Abnormal
PLASMACON N, PLASMACON L-1, PLASMACON L-2
| Applicant | R2 Diagnostics, Inc., South Bend IN, US |
| Decision | Substantially Equivalent, Mar 16, 2007 |
| Received | Aug 8, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062306
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.