510(k) K090135 ยท NXV Diagnostic Light, Soft Tissue Detector
TRIMIRA IDENTAFI 3000
| Applicant | Remicalm, LLC, Houston TX, US |
| Decision | Substantially Equivalent, Feb 17, 2009 |
| Received | Jan 21, 2009 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K090135
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.