510(k) K021231 ยท MMW System, Test, Tumor Marker, Monitoring, Bladder
NMP22 BLADDERCHEK KIT, NMP22 CONTROL KIT
| Applicant | Matritech, Inc., Newton MA, US |
| Decision | Substantially Equivalent, Jul 30, 2002 |
| Received | Apr 18, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021231
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.