510(k) K883031 ยท DXJ Display, Cathode-Ray Tube, Medical
Q-CATH RM
| Applicant | Quinton, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Sep 20, 1988 |
| Received | Jul 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883031
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.