510(k) K160328 ยท PGY Display, Diagnostic Radiology
DIVA ZSP2105CMI with QUBYX PerfectLum bundle
| Applicant | The Linden Group Corp, Cedar Knolls NJ, US |
| Decision | Substantially Equivalent, Feb 25, 2016 |
| Received | Feb 5, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160328
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.